rs34946266 is a SNP of the GNPTAB gene. According to some studies variations in the GNPTAB gene have been associated with abnormalities like Mucolipidosis II (MLII; I-cell disease) and mucolipidosis IIIA (MLIIIA; classical pseudo-Hurler polydystrophy) [R].

 

 

rs34946266

Parent Gene: GNPTAB

Importance: 1
Less common allele: C = 0%
More common allele: T = 100%
My Genotype: Log In
Risk Allele: T
Significance: Pathogenic