RS121909574 TFAP2A

Health Risk Chr 6:10404508 snv missense variant
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What This Variant Does
"[OMIM:?]
Associated Conditions
Branchiooculofacial syndrome
Inborn genetic diseases
Chromatinopathy
Branchiooculofacial syndrome
Inborn genetic diseases
Chromatinopathy
Population Frequencies
gnomAD ALL
100%
Other Variants in TFAP2A
rs121909575 rs2532363719 rs2532358223 rs267607108 rs151344525 rs793888540 rs793888541 rs151344530 rs1554111768 rs1554110735
Ask Dr. Hemsworth about this variant