RS151340624 CLCN5

Health Risk Chr X:50090846
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What This Variant Does
"CLNSIG=5
Associated Conditions
X-linked recessive nephrolithiasis with renal failure
CLCN5-related disorder
Proteinuria
low molecular weight
with hypercalciuria and nephrocalcinosis
Dent disease type 1
X-linked recessive nephrolithiasis with renal failure
CLCN5-related disorder
Proteinuria
low molecular weight
with hypercalciuria and nephrocalcinosis
Dent disease type 1
Other Variants in CLCN5
rs151340620 rs151340621 rs151340622 rs151340623 rs151340625 rs151340626 rs151340627 rs1569540520 rs151340628 rs151340629
Ask Dr. Hemsworth about this variant