rs9493150
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9493150(C;C) |
| Make rs9493150(C;G) |
| Make rs9493150(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 131952851 |
| Gene | CTGF |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9493150 |
| dbSNP (classic) | rs9493150 |
| ClinGen | rs9493150 |
| ebi | rs9493150 |
| HLI | rs9493150 |
| Exac | rs9493150 |
| Gnomad | rs9493150 |
| Varsome | rs9493150 |
| LitVar | rs9493150 |
| Map | rs9493150 |
| PheGenI | rs9493150 |
| Biobank | rs9493150 |
| 1000 genomes | rs9493150 |
| hgdp | rs9493150 |
| ensembl | rs9493150 |
| geneview | rs9493150 |
| scholar | rs9493150 |
| rs9493150 | |
| pharmgkb | rs9493150 |
| gwascentral | rs9493150 |
| openSNP | rs9493150 |
| 23andMe | rs9493150 |
| SNPshot | rs9493150 |
| SNPdbe | rs9493150 |
| MSV3d | rs9493150 |
| GWAS Ctlg | rs9493150 |
| GMAF | 0.2548 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19243500] Validation of connective tissue growth factor (CTGF/CCN2) and its gene polymorphisms as noninvasive biomarkers for the assessment of liver fibrosis
[PMID 22045431
] A polymorphism within the connective tissue growth factor (CTGF) gene has no effect on non-invasive markers of beta-cell area and risk of type 2 diabetes
[PMID 19822645] Variants of CTGF are associated with hepatic fibrosis in Chinese, Sudanese, and Brazilians infected with schistosomes.
[PMID 25502877] Investigating the association between polymorphisms in connective tissue growth factor and susceptibility to colon carcinoma
