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rs8056264

From SNPedia

Orientationplus
Stabilizedplus
Make rs8056264(C;C)
Make rs8056264(C;T)
Make rs8056264(T;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position31321334
GeneITGAM
is asnp
is mentioned by
dbSNPrs8056264
ebirs8056264
HLIrs8056264
Exacrs8056264
Varsomers8056264
Maprs8056264
PheGenIrs8056264
hapmaprs8056264
1000 genomesrs8056264
hgdprs8056264
ensemblrs8056264
gopubmedrs8056264
geneviewrs8056264
scholarrs8056264
googlers8056264
pharmgkbrs8056264
gwascentralrs8056264
openSNPrs8056264
23andMers8056264
23andMe allrs8056264
SNP Nexus

SNPshotrs8056264
SNPdbers8056264
MSV3drs8056264
GWAS Ctlgrs8056264
Max Magnitude
? (C;C) (C;T) (T;T) 28
Although based on a relatively small study, there's a strong association (odds ratios above 30) between the very rare (and neighboring) minor alleles of rs8056264 and rs929867 with common variable immunodeficiency (CVID) reported in [PMID 25678086].