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

rs151341171

From SNPedia

Merged intors12721803
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341171(A;A)
Make rs151341171(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356774
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341171
ebirs151341171
HLIrs151341171
Exacrs151341171
Varsomers151341171
Maprs151341171
PheGenIrs151341171
hapmaprs151341171
1000 genomesrs151341171
hgdprs151341171
ensemblrs151341171
gopubmedrs151341171
geneviewrs151341171
scholarrs151341171
googlers151341171
pharmgkbrs151341171
gwascentralrs151341171
openSNPrs151341171
23andMers151341171
23andMe allrs151341171
SNP Nexus

SNPshotrs151341171
SNPdbers151341171
MSV3drs151341171
GWAS Ctlgrs151341171
StatusMerged into rs12721803
Max Magnitude0
ClinVar
Risk rs151341171(A;A)
Alt rs151341171(A;A)
Reference rs151341171(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324551C>T
CLNSRC
CLNACC