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rs1131159

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1131159(C;G)
Make rs1131159(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357115
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs1131159
dbSNP (classic)rs1131159
ClinGenrs1131159
ebirs1131159
HLIrs1131159
Exacrs1131159
Gnomadrs1131159
Varsomers1131159
LitVarrs1131159
Maprs1131159
PheGenIrs1131159
Biobankrs1131159
1000 genomesrs1131159
hgdprs1131159
ensemblrs1131159
geneviewrs1131159
scholarrs1131159
googlers1131159
pharmgkbrs1131159
gwascentralrs1131159
openSNPrs1131159
23andMers1131159
SNPshotrs1131159
SNPdbers1131159
MSV3drs1131159
GWAS Ctlgrs1131159
GMAF0.3756
Max Magnitude0
ClinVar
Risk rs1131159(G;G)
Alt rs1131159(G;G)
Reference Rs1131159(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324892G>C
CLNSRC
CLNACC