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rs151341197

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341197(C;T)
Make rs151341197(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356715
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341197
ebirs151341197
HLIrs151341197
Exacrs151341197
Varsomers151341197
Maprs151341197
PheGenIrs151341197
hapmaprs151341197
1000 genomesrs151341197
hgdprs151341197
ensemblrs151341197
gopubmedrs151341197
geneviewrs151341197
scholarrs151341197
googlers151341197
pharmgkbrs151341197
gwascentralrs151341197
openSNPrs151341197
23andMers151341197
23andMe allrs151341197
SNP Nexus

SNPshotrs151341197
SNPdbers151341197
MSV3drs151341197
GWAS Ctlgrs151341197
Max Magnitude0
ClinVar
Risk rs151341197(T;T)
Alt rs151341197(T;T)
Reference rs151341197(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324492G>A
CLNSRC
CLNACC