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rs11662763

From SNPedia

Orientationplus
Stabilizedplus
Make rs11662763(C;C)
Make rs11662763(C;T)
Make rs11662763(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position5857092
is asnp
is mentioned by
dbSNPrs11662763
ebirs11662763
HLIrs11662763
Exacrs11662763
Varsomers11662763
Maprs11662763
PheGenIrs11662763
hapmaprs11662763
1000 genomesrs11662763
hgdprs11662763
ensemblrs11662763
gopubmedrs11662763
geneviewrs11662763
scholarrs11662763
googlers11662763
pharmgkbrs11662763
gwascentralrs11662763
openSNPrs11662763
23andMers11662763
23andMe allrs11662763
SNP Nexus

SNPshotrs11662763
SNPdbers11662763
MSV3drs11662763
GWAS Ctlgrs11662763
GMAF0.123
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20694011]
Trait
Title Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency
Risk Allele
P-val 0.000005
Odds Ratio 1.56 [1.30-1.89]