RS138680796 ACSF3

Health Risk Chr 16:89145310 snv missense variant
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What This Variant Does
"CLNSIG=5
Associated Conditions
Combined malonic and methylmalonic acidemia
Methylmalonic acidemia
Inborn genetic diseases
Combined malonic and methylmalonic acidemia
Methylmalonic acidemia
Inborn genetic diseases
Population Frequencies
gnomAD ALL
100%
Other Variants in ACSF3
rs141090143 rs387907118 rs150487794 rs387907119 rs140986055 rs387907121 rs370382601 rs757905943 rs761573352 rs752104014
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