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rs151341359

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341359(A;G)
Make rs151341359(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355381
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341359
ebirs151341359
HLIrs151341359
Exacrs151341359
Varsomers151341359
Maprs151341359
PheGenIrs151341359
hapmaprs151341359
1000 genomesrs151341359
hgdprs151341359
ensemblrs151341359
gopubmedrs151341359
geneviewrs151341359
scholarrs151341359
googlers151341359
pharmgkbrs151341359
gwascentralrs151341359
openSNPrs151341359
23andMers151341359
23andMe allrs151341359
SNP Nexus

SNPshotrs151341359
SNPdbers151341359
MSV3drs151341359
GWAS Ctlgrs151341359
Max Magnitude0
ClinVar
Risk rs151341359(G;G)
Alt rs151341359(G;G)
Reference rs151341359(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323158T>C
CLNSRC
CLNACC