RS138480247 MCCC1

Health Risk Chr 3:183022493 snv missense variant
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Associated Conditions
3-methylcrotonyl-CoA carboxylase 1 deficiency
Inborn genetic diseases
3-methylcrotonyl-CoA carboxylase 1 deficiency
Inborn genetic diseases
Population Frequencies
gnomAD ALL
0%
1kG AFR
0.7%
1kG ALL
0.2%
1kG AMR
0.1%
1kG EAS
100%
1kG EUR
99.9%
1kG SAS
100%
Other Variants in MCCC1
rs119103212 rs119103213 rs119103214 rs119103215 rs119103216 rs119103217 rs119103218 rs398124350 rs398124351 rs398124352
Ask Dr. Hemsworth about this variant