RS80338915 TFAP2B

Health Risk Chr 6:50838007
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What This Variant Does
"Novel TFAP2B mutations that cause Char syndrome provide a genotype-phenotype correlation. [OMIM:?]
Associated Conditions
Char syndrome
Char syndrome
Other Variants in TFAP2B
rs2533123879 rs2113937986 rs2113952620 rs2113960501 rs2113949539 rs373897654 rs1474152110 rs2533148487 rs1377078499 rs2113920409
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