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rs151341101

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341101(C;T)
Make rs151341101(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356911
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341101
ebirs151341101
HLIrs151341101
Exacrs151341101
Varsomers151341101
Maprs151341101
PheGenIrs151341101
hapmaprs151341101
1000 genomesrs151341101
hgdprs151341101
ensemblrs151341101
gopubmedrs151341101
geneviewrs151341101
scholarrs151341101
googlers151341101
pharmgkbrs151341101
gwascentralrs151341101
openSNPrs151341101
23andMers151341101
23andMe allrs151341101
SNP Nexus

SNPshotrs151341101
SNPdbers151341101
MSV3drs151341101
GWAS Ctlgrs151341101
Max Magnitude0
ClinVar
Risk rs151341101(T;T)
Alt rs151341101(T;T)
Reference rs151341101(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324688G>A
CLNSRC
CLNACC