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rs3129763

From SNPedia

Orientationplus
Stabilizedplus
Make rs3129763(A;A)
Make rs3129763(A;G)
Make rs3129763(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position32623148
is asnp
is mentioned by
dbSNPrs3129763
ebirs3129763
HLIrs3129763
Exacrs3129763
Varsomers3129763
Maprs3129763
PheGenIrs3129763
hapmaprs3129763
1000 genomesrs3129763
hgdprs3129763
ensemblrs3129763
gopubmedrs3129763
geneviewrs3129763
scholarrs3129763
googlers3129763
pharmgkbrs3129763
gwascentralrs3129763
openSNPrs3129763
23andMers3129763
23andMe allrs3129763
SNP Nexus

SNPshotrs3129763
SNPdbers3129763
MSV3drs3129763
GWAS Ctlgrs3129763
GMAF0.2094
Max Magnitude
? (A;A) (A;G) (G;G) 28
Source nature

Graves' disease or myasthenia gravis rs3129763(C) + rs4639334(C)

GWAS snp
PMID [PMID 21779181OA-icon.png]
Trait
Title Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.
Risk Allele
P-val 1E-11
Odds Ratio 1.6500 [1.42-1.91]


[PMID 19176549OA-icon.png] Genome-wide association analysis by lasso penalized logistic regression.