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rs151341082

From SNPedia

Merged intors41552714
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341082(C;T)
Make rs151341082(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356979
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341082
ebirs151341082
HLIrs151341082
Exacrs151341082
Varsomers151341082
Maprs151341082
PheGenIrs151341082
hapmaprs151341082
1000 genomesrs151341082
hgdprs151341082
ensemblrs151341082
gopubmedrs151341082
geneviewrs151341082
scholarrs151341082
googlers151341082
pharmgkbrs151341082
gwascentralrs151341082
openSNPrs151341082
23andMers151341082
23andMe allrs151341082
SNP Nexus

SNPshotrs151341082
SNPdbers151341082
MSV3drs151341082
GWAS Ctlgrs151341082
StatusMerged into rs41552714
Max Magnitude0
ClinVar
Risk rs151341082(T;T)
Alt rs151341082(T;T)
Reference rs151341082(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324756G>A
CLNSRC
CLNACC