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rs151341179

From SNPedia

Merged intors1065386
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341179(C;T)
Make rs151341179(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356770
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341179
ebirs151341179
HLIrs151341179
Exacrs151341179
Varsomers151341179
Maprs151341179
PheGenIrs151341179
hapmaprs151341179
1000 genomesrs151341179
hgdprs151341179
ensemblrs151341179
gopubmedrs151341179
geneviewrs151341179
scholarrs151341179
googlers151341179
pharmgkbrs151341179
gwascentralrs151341179
openSNPrs151341179
23andMers151341179
23andMe allrs151341179
SNP Nexus

SNPshotrs151341179
SNPdbers151341179
MSV3drs151341179
GWAS Ctlgrs151341179
StatusMerged into rs1065386
Max Magnitude0
ClinVar
Risk rs151341179(T;T)
Alt rs151341179(T;T)
Reference rs151341179(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324547G>A
CLNSRC
CLNACC