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rs1130838

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1130838(A;G)
Make rs1130838(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269347
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1130838
ebirs1130838
HLIrs1130838
Exacrs1130838
Varsomers1130838
Maprs1130838
PheGenIrs1130838
hapmaprs1130838
1000 genomesrs1130838
hgdprs1130838
ensemblrs1130838
gopubmedrs1130838
geneviewrs1130838
scholarrs1130838
googlers1130838
pharmgkbrs1130838
gwascentralrs1130838
openSNPrs1130838
23andMers1130838
23andMe allrs1130838
SNP Nexus

SNPshotrs1130838
SNPdbers1130838
MSV3drs1130838
GWAS Ctlgrs1130838
GMAF0.2204
Max Magnitude0
ClinVar
Risk rs1130838(G;G)
Alt rs1130838(G;G)
Reference rs1130838(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237124T>C
CLNSRC
CLNACC


[PMID 22201026] Genome-wide pathway analysis of a genome-wide association study on psoriasis and Behcet's disease.