Searches , social queries for SNPEDIA
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Search references for SNPEDIA. Phrases containing SNPEDIA
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Wiki about DNA variations
SNPedia (pronounced "snipedia") is a wiki-based bioinformatics web site that serves as a database of single nucleotide polymorphisms (SNPs). Each article
SNPedia
SNRI antidepressant
3109/00048679809062742. PMID 9588310. S2CID 34824025. "Rs2032583 -SNPedia". Snpedia.com. Archived from the original on 11 December 2013. Retrieved 21
Venlafaxine
Scholarpedia". www.scholarpedia.org. Retrieved 2021-05-01. "Statistics". SNPedia. Archived from the original on February 10, 2016. Retrieved April 21, 2016
List_of_wikis
Effect of alcohol consumption on the human body
PMID 18033686. "rs671 is a classic SNP (Single Nucleotide Polymorphism)". SNPedia. 18 November 2020. Archived from the original on 2018-10-22. "Esophageal
Alcohol_flush_reaction
Lipid-lowering medication
Foster City, CA: Biomedical Publications. pp. 1431–3. "rs4149056 - SNPedia". www.snpedia.com. Archived from the original on 11 January 2009. Link E, Parish
Simvastatin
personal genetic report by comparing a user's DNA data file against the SNPedia database. Web application Proprietary MyHeritage TINKER A molecular dynamics
List of proprietary bioinformatics software
List_of_proprietary_bioinformatics_software
Study of the role of the genome in drug response
Archived from the original on June 14, 2009. "SNPedia". Cariaso M, Lennon G (January 2012). "SNPedia: a wiki supporting personal genome annotation, interpretation
Pharmacogenomics
Medical condition
Leiden, Arg506Gln, R506Q, G1691A Gene Factor V Chromosome 1 External databases Ensembl Human SNPView dbSNP 6025 HapMap 6025 SNPedia 6025 ALFRED SI001216K
Factor_V_Leiden
Free and open-source wiki software
MediaWiki. Other public wikis that run on MediaWiki include wikiHow and SNPedia. WikiLeaks began as a MediaWiki-based site, but is no longer a wiki. A
MediaWiki
Genetic variant
Region Exon 3 External databases Ensembl Human SNPView dbSNP 4680 HapMap 4680 SNPedia 4680 AlzGene Meta-analysis Overview SzGene Meta-analysis Overview
Rs4680
OpenStreetMap Wiki". wiki.openstreetmap.org. Retrieved 7 July 2018. "SNPedia:Copyrights". SNPedia. Retrieved November 15, 2013. Michael Mrozek (2016-11-20). "Power
List of major Creative Commons–licensed works
List_of_major_Creative_Commons–licensed_works
Genetic variation in the MTHFR gene
1 External databases Ensembl Human SNPView dbSNP 1801133 HapMap 1801133 SNPedia 1801133 AlzGene Meta-analysis Overview SzGene Meta-analysis Overview
Rs1801133
Region Promoter External databases Ensembl Human SNPView dbSNP 1800955 HapMap 1800955 SNPedia 1800955 ALFRED SI000215I SzGene Meta-analysis Overview
Rs1800955
DNA-based genetic test
August 2019. Retrieved 8 August 2019. "List of medical conditions – SNPedia". www.snpedia.com. Retrieved 27 June 2019. "The Pros and Cons of the Main Autosomal
Genealogical_DNA_test
Medical condition
SNP: rs1799963 Gene F2 Chromosome 11 External databases Ensembl Human SNPView dbSNP 1799963 HapMap 1799963 SNPedia 1799963
Prothrombin_G20210A
Single nucleotide polymorphism in human BDNF gene
Chromosome 11 External databases Ensembl Human SNPView dbSNP 6265 HapMap 6265 SNPedia 6265 AlzGene Meta-analysis Overview SzGene Meta-analysis Overview PDGene
Rs6265
Group of isomers
Organic Syntheses. 23: 78. doi:10.15227/orgsyn.023.0078. "rs6591536". SNPedia. Jaeger SR, McRae JF, Bava CM, Beresford MK, Hunter D, Jia Y, Chheang SL
Ionone
Single nucleotide polymorphism in human HTR2A gene
Exon 1 External databases Ensembl Human SNPView dbSNP 6313 HapMap 6313 SNPedia 6313 ALFRED SI000324J AlzGene Meta-analysis Overview SzGene Meta-analysis
Rs6313
Medical condition
doi:10.1371/journal.pone.0033222. PMC 3310006. PMID 22470444. https://www.snpedia.com/index.php/rs1801131 consulted 30.10.2023 Kang, S. S.; Wong, P. W. (1996-01-26)
Hyperhomocysteinemia
SNP in the SLC45A2 gene
0104367. ISSN 1932-6203. PMC 4122405. PMID 25093503. "rs16891982 - SNPedia". www.snpedia.com. Retrieved 2022-10-01. "rs16891982 RefSNP Report - dbSNP - NCBI"
Rs16891982
Single nucleotide in genomic DNA at which different sequence alternatives exist
Kaviar is a compendium of SNPs from multiple data sources including dbSNP. SNPedia is a wiki-style database supporting personal genome annotation, interpretation
Single-nucleotide polymorphism
Single-nucleotide_polymorphism
Online genealogy platform
On September 7, 2019, MyHeritage announced that they had acquired both SNPedia and Promethease. All non-European raw genetic data files previously uploaded
MyHeritage
Genetic variation in the SLC6A3 gene
SNP: rs28363170 Gene SLC6A3 Chromosome 5 External databases Ensembl Human SNPView dbSNP 28363170 HapMap 28363170 SNPedia 28363170
Rs28363170
Human mitochondrial DNA haplogroup
test Genetic genealogy Human mitochondrial genetics Population genetics SNPedia Achilli A, Rengo C, Magri C, Battaglia V, Olivieri A, Scozzari R, et al
Haplogroup_H_(mtDNA)
Genetic polymorphism
SNP: rs25531 Gene SLC6A4 Chromosome 17 External databases Ensembl Human SNPView dbSNP 25531 HapMap 25531 SNPedia 25531
5-HTTLPR
Mobile genetic element in the primate genome (including human genome)
S2CID 231761522. "SNP in the promoter region of the myeloperoxidase MPO gene". SNPedia. Archived from the original on 2010-05-21. Retrieved 2010-03-14.[unreliable
Alu_element
Software for managing structured data in MediaWiki
Notable public wikis that use SMW include the Metacafe wiki, Web Platform, SNPedia, SKYbrary, Metavid, Familypedia, OpenEI, the Libreplanet wiki, the Free
Semantic_MediaWiki
Genetic variation in the HTR1A gene
rs6295 Name(s) C-1019G, C(-1019)G Gene HTR1A Chromosome 5 Region Promoter External databases Ensembl Human SNPView dbSNP 6295 HapMap 6295 SNPedia 6295
Rs6295
H452Y Gene HTR2A Chromosome 13 Region Exon 3 External databases Ensembl Human SNPView dbSNP 6314 HapMap 6314 SNPedia 6314 SzGene Meta-analysis Overview
Rs6314
Wiki that implements semantic web
Freebase Gardenology.org Math Images Project Metavid NeuroLex OpenEI SKYbrary SNPedia Wikidata Semantic Wikis and Disaster Relief Operations, Soenke Ziesche
Semantic_wiki
A-1438G, G-1438A Gene HTR2A Chromosome 13 External databases Ensembl Human SNPView dbSNP 6311 HapMap 6311 SNPedia 6311 SzGene Meta-analysis Overview
Rs6311
Genetic variation in the HTR6 gene
C267T, 267T/C Gene HTR6 Chromosome 1 External databases Ensembl Human SNPView dbSNP 1805054 HapMap 1805054 SNPedia 1805054 AlzGene Meta-analysis Overview
Rs1805054
Human glycoprotein that binds to androgens and estrogens
1158/1055-9965.EPI-08-0734. PMC 2660245. PMID 19064566. Trkiehl (2011). "SHBG - SNPedia". Retrieved 13 July 2014. Overview of all the structural information available
Sex_hormone–binding_globulin
Human Y-chromosome DNA haplogroup
10, 2007. Retrieved December 20, 2019. "Haplogroup R (Y-DNA) - SNPedia". www.snpedia.com. Archived from the original on May 5, 2018. Retrieved December
Haplogroup_R1a
Cholesterol-transporting protein most notably implicated in Alzheimer's disease
SNP: rs429358 Gene ApoE Chromosome 19 External databases Ensembl Human SNPView dbSNP 429358 HapMap 429358 SNPedia 429358
Apolipoprotein_E
SNP: rs5569 Name(s) A1287G, G1287A Gene SLC6A2 Chromosome 16 Region Exon 9 External databases Ensembl Human SNPView dbSNP 5569 HapMap 5569 SNPedia 5569
Rs5569
Genetic variation in the HTR1A gene
SNP: rs6294 Name(s) G294A Gene HTR1A Chromosome 5 External databases Ensembl Human SNPView dbSNP 6294 HapMap 6294 SNPedia 6294
Rs6294
Human genes project within Wikipedia
Clarke EL, Loguercio S, Su AI (2012). "Linking genes to diseases with a SNPedia-Gene Wiki mashup". Journal of Biomedical Semantics. 3 (Suppl 1) S6. doi:10
Gene_Wiki
norvegicus Saccharomyces Genome Database: genome of the yeast model organism SNPedia SoyBase Database (SoyBase): USDA soybean genetics and genomic database
List_of_biological_databases
DNA tests performed without definite indication
public-domain archive for a broad collection of simple genetic polymorphisms) SNPedia Archived 2019-03-22 at the Wayback Machine (a wiki-based bioinformatics
Elective genetic and genomic testing
Elective_genetic_and_genomic_testing
Metabolic disorder leading to muscle dysfunction
Muscular Dystrophy Association. 18 December 2015. Retrieved 10 June 2017. SNPedia, 2019, rs17602729 (23 October 2021). "Adenosine monophosphate deaminase
Adenosine monophosphate deaminase deficiency type 1
Adenosine_monophosphate_deaminase_deficiency_type_1
Enzyme
ALDH2*2 Name(s) g.42421G>A, Glu504Lys Gene ALDH2 Chromosome 12 Region Exon External databases Ensembl Human SNPView dbSNP 671 HapMap 671 SNPedia 671
ALDH2
Medical condition
doi:10.1016/j.ygeno.2014.11.009. PMID 25479386. "rs10738445 - SNPedia". www.snpedia.com. Retrieved 2022-09-30. Ogura Y, Kou I, Miura S, Takahashi A
Adolescent idiopathic scoliosis
Adolescent_idiopathic_scoliosis
Open source genetics database (2011–2025)
2025. "openSNP". openSNP. Retrieved 20 November 2016. "Obesity - SNPedia". snpedia.com. Retrieved 20 November 2016. "openSNP is creating Science | Patreon"
OpenSNP
Icelandic biopharmaceutical company
Type 2 Diabetes," 15 April 2007 Example of SNPs included in deCODEme in SNPedia New variant added to deCODE AF in company press release, "deCODE Discovers
DeCODE_genetics
Mammalian protein found in humans
Name(s) C385A, c.385C>A, p.Pro129Thr Gene FAAH Chromosome 1 Region Exon External databases Ensembl Human SNPView dbSNP 324420 HapMap 324420 SNPedia 324420
Fatty-acid_amide_hydrolase_1
Set of cytochrome P450 enzymes
(7–8): 311–8. PMID 20857895. "Rs1799853 - SNPedia". "Rs1057910 - SNPedia". "Rs4244285 - SNPedia". "Rs4986893 - SNPedia". Shin, D. J.; Kwon, J; Park, A. R.;
Epoxygenase
Genetics database
NCBI database of genetic variation. Nucleic Acids Research, 29: 308–311. SNPedia HapMap NCBI NHGRI Wheeler DL, Barrett T, Benson DA, et al. (January 2007)
DbSNP
SNP: rs7997012 Gene HTR2A Chromosome 13 Region Intron 2 External databases Ensembl Human SNPView dbSNP 7997012 HapMap 7997012 SNPedia 7997012
Rs7997012
Protein-coding gene in the species Homo sapiens
OR5A1 olfactory receptor, family 5, subfamily A, member 1". "rs6591536". SNPedia. Jaeger SR, McRae JF, Bava CM, Beresford MK, Hunter D, Jia Y, Chheang SL
OR5A1
rs1800532 Name(s) A218C Gene TPH1 Chromosome 11 Region Intron 7 External databases Ensembl Human SNPView dbSNP 1800532 HapMap 1800532 SNPedia 1800532
Rs1800532
Single nucleotide polymorphism in the human GRIK4 gene
SNP: rs1954787 Gene GRIK4 Chromosome 11 External databases Ensembl Human SNPView dbSNP 1954787 HapMap 1954787 SNPedia 1954787
Rs1954787
Protein-coding gene in the species Homo sapiens
002. ISBN 978-0-12-803119-3. PMC 4667791. PMID 26233909. "Rs1290617". SNPedia. "Reference SNP (refSNP) Cluster Report: rs1290620". Curley CR, Monsuur
CYP4F3
RELN Chromosome 7 Region Intron 4 External databases Ensembl Human SNPView dbSNP 7341475 HapMap 7341475 SNPedia 7341475 SzGene Meta-analysis Overview
Rs7341475
Protein-coding gene in the species Homo sapiens
PMC 3180592. PMID 21499988. For more related information on the SNP: SNPedia Dopamine receptor D2; DRD2: OMNI Entry The Human Gene Compendium DRD2:
ANKK1
TPH1 Chromosome 11 Region Intron 7 External databases Ensembl Human SNPView dbSNP 1799913 HapMap 1799913 SNPedia 1799913 SzGene Meta-analysis Overview
Rs1799913
Protein-coding gene in humans
doi:10.1097/FPC.0b013e328336eefe. PMC 3932492. PMID 20130494. "Rs1126742 - SNPedia". Zordoky BN, El-Kadi AO (Mar 2010). "Effect of cytochrome P450 polymorphism
CYP4A11
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