RS193922701 FGF23

Health Risk Chr 12:4379421
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Autosomal dominant hypophosphatemic rickets
Autosomal dominant hypophosphatemic rickets
Other Variants in FGF23
rs753676774 rs1064795205 rs1555096583 rs1220533001 rs531815578 rs566868058 rs754201217 rs2497236074 rs190841442 rs573322878
Ask Dr. Hemsworth about this variant