{{Rsnum
|rsid=9399005
|Gene=CTGF
|Chromosome=6
|position=131947824
|Orientation=plus
|GMAF=0.2911
|Gene_s=TBC1D2B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 55.8 | 33.6 | 10.6
| HCB | 24.8 | 56.9 | 18.2
| JPT | 33.6 | 47.8 | 18.6
| YRI | 87.1 | 12.2 | 0.7
| ASW | 76.8 | 21.4 | 1.8
| CHB | 24.8 | 56.9 | 18.2
| CHD | 36.7 | 41.3 | 22.0
| GIH | 51.5 | 40.6 | 7.9
| LWK | 80.0 | 19.1 | 0.9
| MEX | 50.0 | 41.4 | 8.6
| MKK | 67.3 | 30.1 | 2.6
| TSI | 48.0 | 48.0 | 3.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=19243500
|Title=Validation of connective tissue growth factor (CTGF/CCN2) and its gene polymorphisms as noninvasive biomarkers for the assessment of liver fibrosis
}}

{{PMID Auto
|PMID=20032097
|Title=Association Between a CTGF Gene Polymorphism and Systemic Sclerosis in a French Population
}}

{{PMID Auto
|PMID=19822645
|Title=Variants of CTGF are associated with hepatic fibrosis in Chinese, Sudanese, and Brazilians infected with schistosomes.
|OA=1
}}

{{PMID Auto
|PMID=24121259
|Title=The Influence of CTGF Single-Nucleotide Polymorphisms on Outcomes in Crohn's Disease
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}