RS797044812 CLCN5

Health Risk Chr X:50090127
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Dent disease type 1
Hypophosphatemic rickets
X-linked recessive
Proteinuria
low molecular weight
with hypercalciuria and nephrocalcinosis
X-linked recessive nephrolithiasis with renal failure
Dent disease type 1
Hypophosphatemic rickets
X-linked recessive
Proteinuria
low molecular weight
with hypercalciuria and nephrocalcinosis
X-linked recessive nephrolithiasis with renal failure
Other Variants in CLCN5
rs151340620 rs151340621 rs151340622 rs151340623 rs151340624 rs151340625 rs151340626 rs151340627 rs1569540520 rs151340628
Ask Dr. Hemsworth about this variant