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rs151341350

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341350(C;G)
Make rs151341350(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355497
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341350
dbSNP (classic)rs151341350
ClinGenrs151341350
ebirs151341350
HLIrs151341350
Exacrs151341350
Gnomadrs151341350
Varsomers151341350
LitVarrs151341350
Maprs151341350
PheGenIrs151341350
Biobankrs151341350
1000 genomesrs151341350
hgdprs151341350
ensemblrs151341350
geneviewrs151341350
scholarrs151341350
googlers151341350
pharmgkbrs151341350
gwascentralrs151341350
openSNPrs151341350
23andMers151341350
SNPshotrs151341350
SNPdbers151341350
MSV3drs151341350
GWAS Ctlgrs151341350
Max Magnitude0
ClinVar
Risk rs151341350(G;G)
Alt rs151341350(G;G)
Reference Rs151341350(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323274G>C
CLNSRC
CLNACC