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rs151341256

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341256(A;G)
Make rs151341256(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356304
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341256
dbSNP (classic)rs151341256
ClinGenrs151341256
ebirs151341256
HLIrs151341256
Exacrs151341256
Gnomadrs151341256
Varsomers151341256
LitVarrs151341256
Maprs151341256
PheGenIrs151341256
Biobankrs151341256
1000 genomesrs151341256
hgdprs151341256
ensemblrs151341256
geneviewrs151341256
scholarrs151341256
googlers151341256
pharmgkbrs151341256
gwascentralrs151341256
openSNPrs151341256
23andMers151341256
SNPshotrs151341256
SNPdbers151341256
MSV3drs151341256
GWAS Ctlgrs151341256
Max Magnitude0
ClinVar
Risk rs151341256(G;G) rs151341256(T;T)
Alt rs151341256(G;G) rs151341256(T;T)
Reference Rs151341256(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324081T>A; NC_000006.11:g.31324081T>C
CLNSRC
CLNACC