RS119103212 MCCC1

Health Risk Chr 3:183045521 snv missense variant
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What This Variant Does
"[OMIM:?]
Associated Conditions
3-methylcrotonyl-CoA carboxylase 1 deficiency
Methylcrotonyl-CoA carboxylase deficiency
Inborn genetic diseases
3-methylcrotonyl-CoA carboxylase 1 deficiency
Methylcrotonyl-CoA carboxylase deficiency
Inborn genetic diseases
Population Frequencies
gnomAD ALL
0%
Other Variants in MCCC1
rs119103213 rs119103214 rs119103215 rs119103216 rs119103217 rs119103218 rs398124350 rs398124351 rs398124352 rs398124353
Ask Dr. Hemsworth about this variant