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rs151341338

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs151341338(-;-)
Make rs151341338(-;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355854
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341338
ebirs151341338
HLIrs151341338
Exacrs151341338
Varsomers151341338
Maprs151341338
PheGenIrs151341338
hapmaprs151341338
1000 genomesrs151341338
hgdprs151341338
ensemblrs151341338
gopubmedrs151341338
geneviewrs151341338
scholarrs151341338
googlers151341338
pharmgkbrs151341338
gwascentralrs151341338
openSNPrs151341338
23andMers151341338
23andMe allrs151341338
SNP Nexus

SNPshotrs151341338
SNPdbers151341338
MSV3drs151341338
GWAS Ctlgrs151341338
Max Magnitude0
ClinVar
Risk rs151341338(;)
Alt rs151341338(;)
Reference rs151341338(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323631delA
CLNSRC
CLNACC