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rs151341178

From SNPedia

Merged intors1065386
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341178(C;G)
Make rs151341178(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356770
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341178
ebirs151341178
HLIrs151341178
Exacrs151341178
Varsomers151341178
Maprs151341178
PheGenIrs151341178
hapmaprs151341178
1000 genomesrs151341178
hgdprs151341178
ensemblrs151341178
gopubmedrs151341178
geneviewrs151341178
scholarrs151341178
googlers151341178
pharmgkbrs151341178
gwascentralrs151341178
openSNPrs151341178
23andMers151341178
23andMe allrs151341178
SNP Nexus

SNPshotrs151341178
SNPdbers151341178
MSV3drs151341178
GWAS Ctlgrs151341178
StatusMerged into rs1065386
Max Magnitude0
ClinVar
Risk rs151341178(G;G)
Alt rs151341178(G;G)
Reference rs151341178(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324547G>C
CLNSRC
CLNACC