Have questions? Visit https://www.reddit.com/r/SNPedia

rs151341245

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341245(A;G)
Make rs151341245(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356331
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341245
dbSNP (classic)rs151341245
ClinGenrs151341245
ebirs151341245
HLIrs151341245
Exacrs151341245
Gnomadrs151341245
Varsomers151341245
LitVarrs151341245
Maprs151341245
PheGenIrs151341245
Biobankrs151341245
1000 genomesrs151341245
hgdprs151341245
ensemblrs151341245
geneviewrs151341245
scholarrs151341245
googlers151341245
pharmgkbrs151341245
gwascentralrs151341245
openSNPrs151341245
23andMers151341245
SNPshotrs151341245
SNPdbers151341245
MSV3drs151341245
GWAS Ctlgrs151341245
Max Magnitude0
ClinVar
Risk rs151341245(G;G)
Alt rs151341245(G;G)
Reference Rs151341245(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324108T>C
CLNSRC
CLNACC