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rs151341097

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341097(C;T)
Make rs151341097(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356921
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341097
ebirs151341097
HLIrs151341097
Exacrs151341097
Varsomers151341097
Maprs151341097
PheGenIrs151341097
hapmaprs151341097
1000 genomesrs151341097
hgdprs151341097
ensemblrs151341097
gopubmedrs151341097
geneviewrs151341097
scholarrs151341097
googlers151341097
pharmgkbrs151341097
gwascentralrs151341097
openSNPrs151341097
23andMers151341097
23andMe allrs151341097
SNP Nexus

SNPshotrs151341097
SNPdbers151341097
MSV3drs151341097
GWAS Ctlgrs151341097
Max Magnitude0
ClinVar
Risk rs151341097(T;T)
Alt rs151341097(T;T)
Reference rs151341097(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324698G>A
CLNSRC
CLNACC