RS797044814 CLCN5

Health Risk Chr X:50092130
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Dent disease type 1
X-linked recessive nephrolithiasis with renal failure
Hypophosphatemic rickets
X-linked recessive
Proteinuria
low molecular weight
with hypercalciuria and nephrocalcinosis
Dent disease type 1
X-linked recessive nephrolithiasis with renal failure
Hypophosphatemic rickets
X-linked recessive
Proteinuria
low molecular weight
with hypercalciuria and nephrocalcinosis
Other Variants in CLCN5
rs151340620 rs151340621 rs151340622 rs151340623 rs151340624 rs151340625 rs151340626 rs151340627 rs1569540520 rs151340628
Ask Dr. Hemsworth about this variant