{{Rsnum
|rsid=1379326
|Gene=CSMD1
|Chromosome=8
|position=4760288
|Orientation=minus
|GMAF=0.3421
|Gene_s=CSMD1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 51.4 | 38.7 | 9.9
| HCB | 44.1 | 46.3 | 9.6
| JPT | 49.5 | 45.0 | 5.4
| YRI | 31.9 | 55.3 | 12.8
| ASW | 40.0 | 41.8 | 18.2
| CHB | 44.1 | 46.3 | 9.6
| CHD | 45.3 | 42.5 | 12.3
| GIH | 49.5 | 38.6 | 11.9
| LWK | 33.0 | 45.9 | 21.1
| MEX | 58.6 | 36.2 | 5.2
| MKK | 29.0 | 41.3 | 29.7
| TSI | 50.0 | 44.1 | 5.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23583980
  |Trait=Interstitial lung disease
  |Title=Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.
  |RiskAllele=C
  |Pval=1E-7
  |OR=1.78
  |ORtxt=[1.45-2.19]
  |OA=1
}}

{{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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}