RS781904041 HCFC1

Health Risk Chr X:153950521
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Associated Conditions
Inborn genetic diseases
Methylmalonic acidemia with homocystinuria
type cblX
Inborn genetic diseases
Methylmalonic acidemia with homocystinuria
type cblX
Other Variants in HCFC1
rs398122908 rs318240758 rs397515485 rs397515486 rs397515487 rs398124206 rs201404751 rs199953428 rs797044886 rs782727601
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