RS138845109 KMT2C

Health Risk Chr 7:152176950 snv missense variant
Upload your DNA to see your genotype for this variant.
Associated Conditions
atypical cerebral palsy
KMT2C-related disorder
atypical cerebral palsy
KMT2C-related disorder
Population Frequencies
gnomAD ALL
0%
1kG AFR
98.9%
1kG ALL
0.3%
1kG AMR
0.3%
1kG EAS
100%
1kG EUR
100%
1kG SAS
100%
Other Variants in KMT2C
rs587777073 rs12674022 rs587778491 rs587778494 rs200297010 rs587778495 rs140626076 rs143269206 rs545625106 rs587778510
Ask Dr. Hemsworth about this variant