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Rs10492294

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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
PheGenIrs10492294
nextbiors10492294
hapmaprs10492294
1000 genomesrs10492294
hgdprs10492294
ensemblrs10492294
gopubmedrs10492294
geneviewrs10492294
scholarrs10492294
googlers10492294
pharmgkbrs10492294
gwascentralrs10492294
openSNPrs10492294
23andMers10492294
23andMe allrs10492294
SNP Nexus

SNPshotrs10492294
SNPdbers10492294
MSV3drs10492294
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]