RS104893722 CLDN16

Health Risk Chr 3:190404905
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Primary hypomagnesemia
Primary hypomagnesemia
Other Variants in CLDN16
rs104893720 rs104893721 rs104893723 rs104893724 rs104893725 rs104893727 rs104893728 rs104893729 rs104893730 rs104893731
Ask Dr. Hemsworth about this variant