Have questions? Visit https://www.reddit.com/r/SNPedia

rs151341370

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341370(A;A)
Make rs151341370(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355334
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341370
ebirs151341370
HLIrs151341370
Exacrs151341370
Varsomers151341370
Maprs151341370
PheGenIrs151341370
hapmaprs151341370
1000 genomesrs151341370
hgdprs151341370
ensemblrs151341370
gopubmedrs151341370
geneviewrs151341370
scholarrs151341370
googlers151341370
pharmgkbrs151341370
gwascentralrs151341370
openSNPrs151341370
23andMers151341370
23andMe allrs151341370
SNP Nexus

SNPshotrs151341370
SNPdbers151341370
MSV3drs151341370
GWAS Ctlgrs151341370
Max Magnitude0
ClinVar
Risk rs151341370(A;A)
Alt rs151341370(A;A)
Reference rs151341370(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323111G>T
CLNSRC
CLNACC