RS886041227 PHEX

Health Risk Chr X:22247942
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What This Variant Does
"CLNSIG=5
Associated Conditions
Familial X-linked hypophosphatemic vitamin D refractory rickets
Autosomal dominant hypophosphatemic rickets
Familial X-linked hypophosphatemic vitamin D refractory rickets
Autosomal dominant hypophosphatemic rickets
Other Variants in PHEX
rs2146979490 rs137853268 rs137853269 rs267606945 rs137853270 rs137853271 rs267606946 rs193922454 rs193922455 rs193922456
Ask Dr. Hemsworth about this variant