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rs151341302

From SNPedia

Merged intors151341301
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341302(C;T)
Make rs151341302(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356256
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341302
ebirs151341302
HLIrs151341302
Exacrs151341302
Varsomers151341302
Maprs151341302
PheGenIrs151341302
hapmaprs151341302
1000 genomesrs151341302
hgdprs151341302
ensemblrs151341302
gopubmedrs151341302
geneviewrs151341302
scholarrs151341302
googlers151341302
pharmgkbrs151341302
gwascentralrs151341302
openSNPrs151341302
23andMers151341302
23andMe allrs151341302
SNP Nexus

SNPshotrs151341302
SNPdbers151341302
MSV3drs151341302
GWAS Ctlgrs151341302
StatusMerged into rs151341301
Max Magnitude0
ClinVar
Risk rs151341302(T;T)
Alt rs151341302(T;T)
Reference rs151341302(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324033G>A
CLNSRC
CLNACC