rs1130838
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs1130838(A;G) |
Make rs1130838(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31269347 |
Gene | HLA-C |
is a | snp |
is | mentioned by |
dbSNP | rs1130838 |
dbSNP (classic) | rs1130838 |
ClinGen | rs1130838 |
ebi | rs1130838 |
HLI | rs1130838 |
Exac | rs1130838 |
Gnomad | rs1130838 |
Varsome | rs1130838 |
LitVar | rs1130838 |
Map | rs1130838 |
PheGenI | rs1130838 |
Biobank | rs1130838 |
1000 genomes | rs1130838 |
hgdp | rs1130838 |
ensembl | rs1130838 |
geneview | rs1130838 |
scholar | rs1130838 |
rs1130838 | |
pharmgkb | rs1130838 |
gwascentral | rs1130838 |
openSNP | rs1130838 |
23andMe | rs1130838 |
SNPshot | rs1130838 |
SNPdbe | rs1130838 |
MSV3d | rs1130838 |
GWAS Ctlg | rs1130838 |
GMAF | 0.2204 |
Max Magnitude | 0 |
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.