RS201367228 CLDN16

Health Risk Chr 3:190408389
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Associated Conditions
Primary hypomagnesemia
Inborn genetic diseases
Clear cell carcinoma of kidney
Primary hypomagnesemia
Inborn genetic diseases
Clear cell carcinoma of kidney
Other Variants in CLDN16
rs104893720 rs104893721 rs104893722 rs104893723 rs104893724 rs104893725 rs104893727 rs104893728 rs104893729 rs104893730
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