RS757052602 MCCC2

Health Risk Chr 5:71641068
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What This Variant Does
"CLNSIG=5
Associated Conditions
3-methylcrotonyl-CoA carboxylase 2 deficiency
Methylcrotonyl-CoA carboxylase deficiency
Inborn genetic diseases
MCCC2-related disorder
3-methylcrotonyl-CoA carboxylase 2 deficiency
Methylcrotonyl-CoA carboxylase deficiency
Inborn genetic diseases
MCCC2-related disorder
Other Variants in MCCC2
rs587776533 rs119103219 rs119103220 rs119103221 rs119103222 rs119103223 rs119103224 rs119103225 rs119103226 rs730880265
Ask Dr. Hemsworth about this variant