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rs151341237

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341237(A;A)
Make rs151341237(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356379
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341237
dbSNP (classic)rs151341237
ClinGenrs151341237
ebirs151341237
HLIrs151341237
Exacrs151341237
Gnomadrs151341237
Varsomers151341237
LitVarrs151341237
Maprs151341237
PheGenIrs151341237
Biobankrs151341237
1000 genomesrs151341237
hgdprs151341237
ensemblrs151341237
geneviewrs151341237
scholarrs151341237
googlers151341237
pharmgkbrs151341237
gwascentralrs151341237
openSNPrs151341237
23andMers151341237
SNPshotrs151341237
SNPdbers151341237
MSV3drs151341237
GWAS Ctlgrs151341237
Max Magnitude0
ClinVar
Risk rs151341237(A;A)
Alt rs151341237(A;A)
Reference Rs151341237(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324156C>T
CLNSRC
CLNACC