RS145118503 CLDN16

Health Risk Chr 3:190388351
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Associated Conditions
Primary hypomagnesemia
Inborn genetic diseases
Primary hypomagnesemia
Inborn genetic diseases
Other Variants in CLDN16
rs104893720 rs104893721 rs104893722 rs104893723 rs104893724 rs104893725 rs104893727 rs104893728 rs104893729 rs104893730
Ask Dr. Hemsworth about this variant