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

rs1131217

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1131217(A;G)
Make rs1131217(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356730
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs1131217
dbSNP (classic)rs1131217
ClinGenrs1131217
ebirs1131217
HLIrs1131217
Exacrs1131217
Gnomadrs1131217
Varsomers1131217
LitVarrs1131217
Maprs1131217
PheGenIrs1131217
Biobankrs1131217
1000 genomesrs1131217
hgdprs1131217
ensemblrs1131217
geneviewrs1131217
scholarrs1131217
googlers1131217
pharmgkbrs1131217
gwascentralrs1131217
openSNPrs1131217
23andMers1131217
SNPshotrs1131217
SNPdbers1131217
MSV3drs1131217
GWAS Ctlgrs1131217
Max Magnitude0
ClinVar
Risk rs1131217(G;G) rs1131217(T;T)
Alt rs1131217(G;G) rs1131217(T;T)
Reference Rs1131217(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324507T>A; NC_000006.11:g.31324507T>C
CLNSRC
CLNACC