This SNP has been found in patients with pachyonychia congenita Type I, and the risk allele appears to be a causative mutation for this (dominant) disorder.

See also: OMIM 148067.0008


rs59328451

Parent Gene: KRT16

Importance: 1
Less common allele: A = 0%
More common allele: T = 100%
My Genotype: Log In