rs104893726, CLDN16

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Primary hypomagnesemia (disorder)
CUI: C0268448
Disease: Primary hypomagnesemia (disorder)
22 0.882 0.200 3 190408416 missense variant T/G snv 0.800 1.000 3 1999 2001
Nephrocalcinosis
CUI: C0027709
Disease: Nephrocalcinosis
20 0.882 0.200 3 190408416 missense variant T/G snv 0.700 1.000 1 2018 2018
Nephrolithiasis
CUI: C0392525
Disease: Nephrolithiasis
99 0.882 0.200 3 190408416 missense variant T/G snv 0.700 1.000 1 2018 2018