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rs151341172

From SNPedia

Merged intors12721803
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341172(C;C)
Make rs151341172(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356774
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341172
ebirs151341172
HLIrs151341172
Exacrs151341172
Varsomers151341172
Maprs151341172
PheGenIrs151341172
hapmaprs151341172
1000 genomesrs151341172
hgdprs151341172
ensemblrs151341172
gopubmedrs151341172
geneviewrs151341172
scholarrs151341172
googlers151341172
pharmgkbrs151341172
gwascentralrs151341172
openSNPrs151341172
23andMers151341172
23andMe allrs151341172
SNP Nexus

SNPshotrs151341172
SNPdbers151341172
MSV3drs151341172
GWAS Ctlgrs151341172
StatusMerged into rs12721803
Max Magnitude0
ClinVar
Risk rs151341172(C;C)
Alt rs151341172(C;C)
Reference rs151341172(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324551C>G
CLNSRC
CLNACC