RS398123478 SMPD1

Health Risk Chr 11:6394335
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Niemann-Pick disease
type A
type B
Sphingomyelin/cholesterol lipidosis
See cases
type C1
Niemann-Pick disease
type A
type B
Sphingomyelin/cholesterol lipidosis
See cases
type C1
Other Variants in SMPD1
rs120074117 rs120074119 rs267607073 rs120074120 rs120074121 rs120074122 rs120074123 rs120074124 rs387906289 rs120074125
Ask Dr. Hemsworth about this variant