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rs151341202

From SNPedia

Merged intors151341201
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341202(C;G)
Make rs151341202(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356704
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341202
ebirs151341202
HLIrs151341202
Exacrs151341202
Varsomers151341202
Maprs151341202
PheGenIrs151341202
hapmaprs151341202
1000 genomesrs151341202
hgdprs151341202
ensemblrs151341202
gopubmedrs151341202
geneviewrs151341202
scholarrs151341202
googlers151341202
pharmgkbrs151341202
gwascentralrs151341202
openSNPrs151341202
23andMers151341202
23andMe allrs151341202
SNP Nexus

SNPshotrs151341202
SNPdbers151341202
MSV3drs151341202
GWAS Ctlgrs151341202
StatusMerged into rs151341201
Max Magnitude0
ClinVar
Risk rs151341202(G;G)
Alt rs151341202(G;G)
Reference rs151341202(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324481G>C
CLNSRC
CLNACC