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rs151341241

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs151341241(C;C)
Make rs151341241(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356362
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341241
dbSNP (old)rs151341241
ClinGenrs151341241
ebirs151341241
HLIrs151341241
Exacrs151341241
Varsomers151341241
Maprs151341241
PheGenIrs151341241
Biobankrs151341241
1000 genomesrs151341241
hgdprs151341241
ensemblrs151341241
gopubmedrs151341241
geneviewrs151341241
scholarrs151341241
googlers151341241
pharmgkbrs151341241
gwascentralrs151341241
openSNPrs151341241
23andMers151341241
23andMe allrs151341241
SNP Nexus

SNPshotrs151341241
SNPdbers151341241
MSV3drs151341241
GWAS Ctlgrs151341241
Max Magnitude0
ClinVar
Risk rs151341241(C;C)
Alt rs151341241(C;C)
Reference Rs151341241(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324139A>G
CLNSRC
CLNACC