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rs1131292

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1131292(C;T)
Make rs1131292(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270469
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1131292
dbSNP (classic)rs1131292
ClinGenrs1131292
ebirs1131292
HLIrs1131292
Exacrs1131292
Gnomadrs1131292
Varsomers1131292
LitVarrs1131292
Maprs1131292
PheGenIrs1131292
Biobankrs1131292
1000 genomesrs1131292
hgdprs1131292
ensemblrs1131292
geneviewrs1131292
scholarrs1131292
googlers1131292
pharmgkbrs1131292
gwascentralrs1131292
openSNPrs1131292
23andMers1131292
SNPshotrs1131292
SNPdbers1131292
MSV3drs1131292
GWAS Ctlgrs1131292
Max Magnitude0
ClinVar
Risk rs1131292(T;T)
Alt rs1131292(T;T)
Reference Rs1131292(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238246G>A
CLNSRC
CLNACC