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rs587776775

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776775(A;A)
Make rs587776775(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2395971
GeneCD81
is asnp
is mentioned by
dbSNPrs587776775
ebirs587776775
HLIrs587776775
Exacrs587776775
Varsomers587776775
Maprs587776775
PheGenIrs587776775
hapmaprs587776775
1000 genomesrs587776775
hgdprs587776775
ensemblrs587776775
gopubmedrs587776775
geneviewrs587776775
scholarrs587776775
googlers587776775
pharmgkbrs587776775
gwascentralrs587776775
openSNPrs587776775
23andMers587776775
23andMe allrs587776775
SNP Nexus

SNPshotrs587776775
SNPdbers587776775
MSV3drs587776775
GWAS Ctlgrs587776775
Max Magnitude0
ClinVar
Risk rs587776775(A;A)
Alt rs587776775(A;A)
Reference rs587776775(G;G)
Significance Pathogenic
Disease IMMUNODEFICIENCY
Variation info
Gene CD81
CLNDBN IMMUNODEFICIENCY, COMMON VARIABLE, 6 (1 patient)
Reversed 0
HGVS NC_000011.9:g.2417201G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013580.25,