RS111250264 CHD8

Health Risk Chr 14:21431302 snv missense variant
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Population Frequencies
gnomAD ALL
0%
1kG AFR
99.5%
1kG ALL
99.9%
1kG AMR
100%
1kG EAS
100%
1kG EUR
100%
1kG SAS
100%
Other Variants in CHD8
rs1331026006 rs2139484859 rs1594344233 rs397514551 rs397514552 rs1887639311 rs1887627866 rs61752839 rs377595194 rs794727436
Ask Dr. Hemsworth about this variant