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rs151341310

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341310(A;G)
Make rs151341310(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356245
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341310
dbSNP (classic)rs151341310
ClinGenrs151341310
ebirs151341310
HLIrs151341310
Exacrs151341310
Gnomadrs151341310
Varsomers151341310
LitVarrs151341310
Maprs151341310
PheGenIrs151341310
Biobankrs151341310
1000 genomesrs151341310
hgdprs151341310
ensemblrs151341310
geneviewrs151341310
scholarrs151341310
googlers151341310
pharmgkbrs151341310
gwascentralrs151341310
openSNPrs151341310
23andMers151341310
SNPshotrs151341310
SNPdbers151341310
MSV3drs151341310
GWAS Ctlgrs151341310
Max Magnitude0
ClinVar
Risk rs151341310(G;G)
Alt rs151341310(G;G)
Reference Rs151341310(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324022T>C
CLNSRC
CLNACC