rs9399005
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs9399005(C;T) |
| Make rs9399005(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 131947824 |
| Gene | CTGF |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9399005 |
| dbSNP (classic) | rs9399005 |
| ClinGen | rs9399005 |
| ebi | rs9399005 |
| HLI | rs9399005 |
| Exac | rs9399005 |
| Gnomad | rs9399005 |
| Varsome | rs9399005 |
| LitVar | rs9399005 |
| Map | rs9399005 |
| PheGenI | rs9399005 |
| Biobank | rs9399005 |
| 1000 genomes | rs9399005 |
| hgdp | rs9399005 |
| ensembl | rs9399005 |
| geneview | rs9399005 |
| scholar | rs9399005 |
| rs9399005 | |
| pharmgkb | rs9399005 |
| gwascentral | rs9399005 |
| openSNP | rs9399005 |
| 23andMe | rs9399005 |
| SNPshot | rs9399005 |
| SNPdbe | rs9399005 |
| MSV3d | rs9399005 |
| GWAS Ctlg | rs9399005 |
| GMAF | 0.2911 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 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 20032097] Association Between a CTGF Gene Polymorphism and Systemic Sclerosis in a French Population
[PMID 19822645
] Variants of CTGF are associated with hepatic fibrosis in Chinese, Sudanese, and Brazilians infected with schistosomes.
[PMID 24121259] The Influence of CTGF Single-Nucleotide Polymorphisms on Outcomes in Crohn's Disease
[PMID 25502877] Investigating the association between polymorphisms in connective tissue growth factor and susceptibility to colon carcinoma
