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

rs1131096

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1131096(A;A)
Make rs1131096(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270482
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1131096
ebirs1131096
HLIrs1131096
Exacrs1131096
Varsomers1131096
Maprs1131096
PheGenIrs1131096
hapmaprs1131096
1000 genomesrs1131096
hgdprs1131096
ensemblrs1131096
gopubmedrs1131096
geneviewrs1131096
scholarrs1131096
googlers1131096
pharmgkbrs1131096
gwascentralrs1131096
openSNPrs1131096
23andMers1131096
23andMe allrs1131096
SNP Nexus

SNPshotrs1131096
SNPdbers1131096
MSV3drs1131096
GWAS Ctlgrs1131096
GMAF0.225
Max Magnitude0
ClinVar
Risk rs1131096(A,G;A,G)
Alt rs1131096(A,G;A,G)
Reference rs1131096(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238259G>C; NC_000006.11:g.31238259G>T
CLNSRC
CLNACC