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rs151341144

From SNPedia

Merged intors1050556
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341144(C;C)
Make rs151341144(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356809
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341144
ebirs151341144
HLIrs151341144
Exacrs151341144
Varsomers151341144
Maprs151341144
PheGenIrs151341144
hapmaprs151341144
1000 genomesrs151341144
hgdprs151341144
ensemblrs151341144
gopubmedrs151341144
geneviewrs151341144
scholarrs151341144
googlers151341144
pharmgkbrs151341144
gwascentralrs151341144
openSNPrs151341144
23andMers151341144
23andMe allrs151341144
SNP Nexus

SNPshotrs151341144
SNPdbers151341144
MSV3drs151341144
GWAS Ctlgrs151341144
StatusMerged into rs1050556
Max Magnitude0
ClinVar
Risk rs151341144(C;C)
Alt rs151341144(C;C)
Reference rs151341144(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324586C>G
CLNSRC
CLNACC