RS151340627 CLCN5

Health Risk Chr X:50086551
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What This Variant Does
"[OMIM:?]
Associated Conditions
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
Dent disease type 1
Hypophosphatemic rickets
X-linked recessive
Other Variants in CLCN5
rs151340620 rs151340621 rs151340622 rs151340623 rs151340624 rs151340625 rs151340626 rs1569540520 rs151340628 rs151340629
Ask Dr. Hemsworth about this variant