[PMID 23271051] 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

[PMID 18520591] Sequence variants in host cell factor C1 are associated with Meniere's disease.

[PMID 19938081] Altered transmission of HOX and apoptotic SNPs identify a potential common pathway for clubfoot.


Parent Gene: CASP3

Importance: 1
Less common allele: G = 8%
More common allele: A = 92%
My Genotype: Log In