{{Rsnum
|rsid=1049253
|Gene=CASP3
|Chromosome=4
|position=184627797
|Orientation=plus
|GMAF=0.08861
|Gene_s=CASP3
|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 | 4.5 | 25.0 | 70.5
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 0.0 | 100.0
| ASW | 1.8 | 10.5 | 87.7
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 1.0 | 16.8 | 82.2
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 10.5 | 89.5
| MKK | 0.0 | 7.1 | 92.9
| TSI | 2.0 | 37.3 | 60.8
| HapMapRevision=28
}}{{PMID Auto
|PMID=23271051
|Title=A functional variant at the miR-885-5p binding site of CASP3 confers risk of both index and second primary malignancies in patients with head and neck cancer
|OA=1
}}

{{PMID Auto
|PMID=18520591
|Title=Sequence variants in host cell factor C1 are associated with Meniere's disease.
|OA=1
}}

{{PMID Auto
|PMID=19938081
|Title=Altered transmission of HOX and apoptotic SNPs identify a potential common pathway for clubfoot.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}