rs11047102
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11047102(C;C) |
Make rs11047102(C;T) |
Make rs11047102(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 23793212 |
Gene | SOX5 |
is a | snp |
is | mentioned by |
dbSNP | rs11047102 |
dbSNP (classic) | rs11047102 |
ClinGen | rs11047102 |
ebi | rs11047102 |
HLI | rs11047102 |
Exac | rs11047102 |
Gnomad | rs11047102 |
Varsome | rs11047102 |
LitVar | rs11047102 |
Map | rs11047102 |
PheGenI | rs11047102 |
Biobank | rs11047102 |
1000 genomes | rs11047102 |
hgdp | rs11047102 |
ensembl | rs11047102 |
geneview | rs11047102 |
scholar | rs11047102 |
rs11047102 | |
pharmgkb | rs11047102 |
gwascentral | rs11047102 |
openSNP | rs11047102 |
23andMe | rs11047102 |
SNPshot | rs11047102 |
SNPdbe | rs11047102 |
MSV3d | rs11047102 |
GWAS Ctlg | rs11047102 |
GMAF | 0.0753 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21779181] |
Trait | |
Title | Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy. |
Risk Allele | |
P-val | 1E-7 |
Odds Ratio | 1.3600 [1.21-1.52] |
rs11047102 is associated with systemic sclerosis. [PMID 21779181]