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rs10492294

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs10492294(C;C)
Make rs10492294(C;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position128234169
is asnp
is mentioned by
dbSNPrs10492294
dbSNP (classic)rs10492294
ClinGenrs10492294
ebirs10492294
HLIrs10492294
Exacrs10492294
Gnomadrs10492294
Varsomers10492294
LitVarrs10492294
Maprs10492294
PheGenIrs10492294
Biobankrs10492294
1000 genomesrs10492294
hgdprs10492294
ensemblrs10492294
geneviewrs10492294
scholarrs10492294
googlers10492294
pharmgkbrs10492294
gwascentralrs10492294
openSNPrs10492294
23andMers10492294
SNPshotrs10492294
SNPdbers10492294
MSV3drs10492294
GWAS Ctlgrs10492294
GMAF0.1598
Max Magnitude0
? (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 0.000004
Odds Ratio 1.49 [1.27-1.75]