RS397515487 HCFC1
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Methylmalonic acidemia with homocystinuria
type cblX
Disorders of Intracellular Cobalamin Metabolism
Methylmalonic acidemia with homocystinuria
type cblX
Disorders of Intracellular Cobalamin Metabolism
Other Variants in HCFC1