RS765766600 SLC34A1
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Associated Conditions
Inborn genetic diseases
Hypercalcemia
infantile
2
Hypophosphatemic nephrolithiasis/osteoporosis 1
Inborn genetic diseases
Hypercalcemia
infantile
2
Hypophosphatemic nephrolithiasis/osteoporosis 1
Other Variants in SLC34A1