RS876661331 FGF8

Health Risk Chr 10:101770447
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What This Variant Does
"CLNSIG=4
Associated Conditions
Holoprosencephaly sequence
See cases
Holoprosencephaly sequence
See cases
Other Variants in FGF8
rs781205876 rs1554834892 rs139565972 rs1554834321 rs61730334 rs1554834889 rs2539366540 rs769756528 rs537681304 rs1554834303
Ask Dr. Hemsworth about this variant