{{Rsnum
|rsid=12526196
|Gene=LOC100131774
|Chromosome=6
|position=131942336
|Orientation=plus
|GMAF=0.1102
|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 | 1.8 | 8.9 | 89.3
| HCB | 5.1 | 30.7 | 64.2
| JPT | 3.5 | 26.5 | 69.9
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 5.1 | 30.7 | 64.2
| CHD | 0.9 | 38.5 | 60.6
| GIH | 14.9 | 46.5 | 38.6
| LWK | 0.0 | 2.7 | 97.3
| MEX | 0.0 | 24.6 | 75.4
| MKK | 0.0 | 9.0 | 91.0
| TSI | 2.0 | 31.4 | 66.7
| HapMapRevision=28
}}{{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}}