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rs151341118

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341118(G;T)
Make rs151341118(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356841
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341118
dbSNP (classic)rs151341118
ClinGenrs151341118
ebirs151341118
HLIrs151341118
Exacrs151341118
Gnomadrs151341118
Varsomers151341118
LitVarrs151341118
Maprs151341118
PheGenIrs151341118
Biobankrs151341118
1000 genomesrs151341118
hgdprs151341118
ensemblrs151341118
geneviewrs151341118
scholarrs151341118
googlers151341118
pharmgkbrs151341118
gwascentralrs151341118
openSNPrs151341118
23andMers151341118
SNPshotrs151341118
SNPdbers151341118
MSV3drs151341118
GWAS Ctlgrs151341118
Max Magnitude0
ClinVar
Risk rs151341118(T;T)
Alt rs151341118(T;T)
Reference Rs151341118(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324618C>A
CLNSRC
CLNACC