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rs151341140

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341140(C;T)
Make rs151341140(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356810
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341140
ebirs151341140
HLIrs151341140
Exacrs151341140
Varsomers151341140
Maprs151341140
PheGenIrs151341140
hapmaprs151341140
1000 genomesrs151341140
hgdprs151341140
ensemblrs151341140
gopubmedrs151341140
geneviewrs151341140
scholarrs151341140
googlers151341140
pharmgkbrs151341140
gwascentralrs151341140
openSNPrs151341140
23andMers151341140
23andMe allrs151341140
SNP Nexus

SNPshotrs151341140
SNPdbers151341140
MSV3drs151341140
GWAS Ctlgrs151341140
Merged fromRs151341141
Max Magnitude0
ClinVar
Risk rs151341140(G,T;G,T)
Alt rs151341140(G,T;G,T)
Reference rs151341140(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324587G>A; NC_000006.11:g.31324587G>C
CLNSRC
CLNACC