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rs151341198

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341198(A;A)
Make rs151341198(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356710
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341198
ebirs151341198
HLIrs151341198
Exacrs151341198
Varsomers151341198
Maprs151341198
PheGenIrs151341198
hapmaprs151341198
1000 genomesrs151341198
hgdprs151341198
ensemblrs151341198
gopubmedrs151341198
geneviewrs151341198
scholarrs151341198
googlers151341198
pharmgkbrs151341198
gwascentralrs151341198
openSNPrs151341198
23andMers151341198
23andMe allrs151341198
SNP Nexus

SNPshotrs151341198
SNPdbers151341198
MSV3drs151341198
GWAS Ctlgrs151341198
Max Magnitude0
ClinVar
Risk rs151341198(A,T;A,T)
Alt rs151341198(A,T;A,T)
Reference rs151341198(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324487G>A; NC_000006.11:g.31324487G>T
CLNSRC
CLNACC