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rs3926873

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs3926873(A;A)
Make rs3926873(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354563
GeneHLA-B
is asnp
is mentioned by
dbSNPrs3926873
ebirs3926873
HLIrs3926873
Exacrs3926873
Varsomers3926873
Maprs3926873
PheGenIrs3926873
hapmaprs3926873
1000 genomesrs3926873
hgdprs3926873
ensemblrs3926873
gopubmedrs3926873
geneviewrs3926873
scholarrs3926873
googlers3926873
pharmgkbrs3926873
gwascentralrs3926873
openSNPrs3926873
23andMers3926873
23andMe allrs3926873
SNP Nexus

SNPshotrs3926873
SNPdbers3926873
MSV3drs3926873
GWAS Ctlgrs3926873
GMAF0.0753
Max Magnitude0
ClinVar
Risk rs3926873(A,T;A,T)
Alt rs3926873(A,T;A,T)
Reference rs3926873(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322340G>A; NC_000006.11:g.31322340G>T
CLNSRC
CLNACC