RS121909574 TFAP2A

Health Risk Chr 6:10404509
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What This Variant Does
"[OMIM:?]
Associated Conditions
Branchiooculofacial syndrome
Inborn genetic diseases
Chromatinopathy
Branchiooculofacial syndrome
Inborn genetic diseases
Chromatinopathy
Other Variants in TFAP2A
rs121909575 rs2532363719 rs2532358223 rs267607108 rs151344525 rs793888540 rs793888541 rs151344530 rs1554111768 rs1554110735
Ask Dr. Hemsworth about this variant