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rs151341348

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341348(C;T)
Make rs151341348(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355513
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341348
ebirs151341348
HLIrs151341348
Exacrs151341348
Varsomers151341348
Maprs151341348
PheGenIrs151341348
hapmaprs151341348
1000 genomesrs151341348
hgdprs151341348
ensemblrs151341348
gopubmedrs151341348
geneviewrs151341348
scholarrs151341348
googlers151341348
pharmgkbrs151341348
gwascentralrs151341348
openSNPrs151341348
23andMers151341348
23andMe allrs151341348
SNP Nexus

SNPshotrs151341348
SNPdbers151341348
MSV3drs151341348
GWAS Ctlgrs151341348
Max Magnitude0
ClinVar
Risk rs151341348(T;T)
Alt rs151341348(T;T)
Reference rs151341348(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323290G>A
CLNSRC
CLNACC