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rs151341216

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341216(A;T)
Make rs151341216(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356422
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341216
dbSNP (classic)rs151341216
ClinGenrs151341216
ebirs151341216
HLIrs151341216
Exacrs151341216
Gnomadrs151341216
Varsomers151341216
LitVarrs151341216
Maprs151341216
PheGenIrs151341216
Biobankrs151341216
1000 genomesrs151341216
hgdprs151341216
ensemblrs151341216
geneviewrs151341216
scholarrs151341216
googlers151341216
pharmgkbrs151341216
gwascentralrs151341216
openSNPrs151341216
23andMers151341216
SNPshotrs151341216
SNPdbers151341216
MSV3drs151341216
GWAS Ctlgrs151341216
Max Magnitude0
ClinVar
Risk rs151341216(C;C) rs151341216(T;T)
Alt rs151341216(C;C) rs151341216(T;T)
Reference Rs151341216(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324199T>A; NC_000006.11:g.31324199T>G
CLNSRC
CLNACC