RS765478662 FGF23

Health Risk Chr 12:4370768
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Associated Conditions
Autosomal dominant hypophosphatemic rickets
Tumoral calcinosis
hyperphosphatemic
familial
2
Inborn genetic diseases
Autosomal dominant hypophosphatemic rickets
Tumoral calcinosis
hyperphosphatemic
familial
2
Inborn genetic diseases
Other Variants in FGF23
rs753676774 rs1064795205 rs1555096583 rs1220533001 rs531815578 rs566868058 rs754201217 rs2497236074 rs190841442 rs573322878
Ask Dr. Hemsworth about this variant