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rs3130501

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs3130501(A;A)
Make rs3130501(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31168676
GenePOU5F1
is asnp
is mentioned by
dbSNPrs3130501
dbSNP (classic)rs3130501
ClinGenrs3130501
ebirs3130501
HLIrs3130501
Exacrs3130501
Gnomadrs3130501
Varsomers3130501
LitVarrs3130501
Maprs3130501
PheGenIrs3130501
Biobankrs3130501
1000 genomesrs3130501
hgdprs3130501
ensemblrs3130501
geneviewrs3130501
scholarrs3130501
googlers3130501
pharmgkbrs3130501
gwascentralrs3130501
openSNPrs3130501
23andMers3130501
SNPshotrs3130501
SNPdbers3130501
MSV3drs3130501
GWAS Ctlgrs3130501
GMAF0.2296
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 21801394OA-icon.png]
Trait
Title Genome-Wide Association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe.
Risk Allele G
P-val 2E-8
Odds Ratio 1.7400 [1.43-2.13]

[PMID 17660530] Risk alleles for multiple sclerosis identified by a genomewide study.


[PMID 26049586] A human leukocyte antigen locus haplotype confers risk for allopurinol-related adverse effects in Caucasian patients with gout