RS876661328 FGF8

Health Risk Chr 10:101774752
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Semilobar holoprosencephaly
Semilobar holoprosencephaly
Other Variants in FGF8
rs781205876 rs1554834892 rs139565972 rs1554834321 rs61730334 rs1554834889 rs2539366540 rs769756528 rs537681304 rs1554834303
Ask Dr. Hemsworth about this variant