RS1933979876 CLCN5
Upload your DNA to see your genotype for this variant.
Associated Conditions
Dent disease type 1
X-linked recessive nephrolithiasis with renal failure
Proteinuria
low molecular weight
with hypercalciuria and nephrocalcinosis
Hypophosphatemic rickets
X-linked recessive
Dent disease type 1
X-linked recessive nephrolithiasis with renal failure
Proteinuria
low molecular weight
with hypercalciuria and nephrocalcinosis
Hypophosphatemic rickets
X-linked recessive
Other Variants in CLCN5