RS139876661 CHD7

Health Risk Chr 8:60856122 snv missense variant
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Associated Conditions
CHARGE syndrome
Inborn genetic diseases
CHARGE syndrome
Inborn genetic diseases
Population Frequencies
gnomAD ALL
100%
1kG AFR
99.8%
1kG ALL
0.1%
1kG AMR
100%
1kG EAS
100%
1kG EUR
100%
1kG SAS
100%
Other Variants in CHD7
rs121434338 rs121434339 rs121434340 rs121434341 rs121434342 rs786200873 rs121434343 rs121434344 rs387906271 rs202143667
Ask Dr. Hemsworth about this variant