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rs151341109

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs151341109(C;C)
Make rs151341109(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356876
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341109
dbSNP (classic)rs151341109
ClinGenrs151341109
ebirs151341109
HLIrs151341109
Exacrs151341109
Gnomadrs151341109
Varsomers151341109
LitVarrs151341109
Maprs151341109
PheGenIrs151341109
Biobankrs151341109
1000 genomesrs151341109
hgdprs151341109
ensemblrs151341109
geneviewrs151341109
scholarrs151341109
googlers151341109
pharmgkbrs151341109
gwascentralrs151341109
openSNPrs151341109
23andMers151341109
SNPshotrs151341109
SNPdbers151341109
MSV3drs151341109
GWAS Ctlgrs151341109
Max Magnitude0
ClinVar
Risk rs151341109(C;C)
Alt rs151341109(C;C)
Reference Rs151341109(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324653A>G
CLNSRC
CLNACC