RS863224872 FGF23

Health Risk Chr 12:4372649
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What This Variant Does
"CLNSIG=4
Associated Conditions
Familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome
Familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome
Other Variants in FGF23
rs753676774 rs1064795205 rs1555096583 rs1220533001 rs531815578 rs566868058 rs754201217 rs2497236074 rs190841442 rs573322878
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