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rs3177891

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs3177891(C;T)
Make rs3177891(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356914
GeneHLA-B
is asnp
is mentioned by
dbSNPrs3177891
ebirs3177891
HLIrs3177891
Exacrs3177891
Varsomers3177891
Maprs3177891
PheGenIrs3177891
hapmaprs3177891
1000 genomesrs3177891
hgdprs3177891
ensemblrs3177891
gopubmedrs3177891
geneviewrs3177891
scholarrs3177891
googlers3177891
pharmgkbrs3177891
gwascentralrs3177891
openSNPrs3177891
23andMers3177891
23andMe allrs3177891
SNP Nexus

SNPshotrs3177891
SNPdbers3177891
MSV3drs3177891
GWAS Ctlgrs3177891
Max Magnitude0
ClinVar
Risk rs3177891(G,T;G,T)
Alt rs3177891(G,T;G,T)
Reference rs3177891(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324691G>A; NC_000006.11:g.31324691G>C
CLNSRC
CLNACC