RS398123474 SMPD1
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Niemann-Pick disease
type A
Sphingomyelin/cholesterol lipidosis
type B
Niemann-Pick disease
type A
Sphingomyelin/cholesterol lipidosis
type B
Other Variants in SMPD1