rs138308105, CLDN16

N. diseases: 7
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.
Hypercalciuria
CUI: C0020438
Disease: Hypercalciuria
5 0.925 0.200 3 190408323 missense variant G/A;C snv 6.8E-05 2.6E-04 0.700 0
Hypermagnesiuria
CUI: C2673443
Disease: Hypermagnesiuria
1 0.925 0.200 3 190408323 missense variant G/A;C snv 6.8E-05 2.6E-04 0.700 0
Hypocitraturia
CUI: C2673444
Disease: Hypocitraturia
2 0.925 0.200 3 190408323 missense variant G/A;C snv 6.8E-05 2.6E-04 0.700 0
Hypomagnesemia
CUI: C0151723
Disease: Hypomagnesemia
11 0.925 0.200 3 190408323 missense variant G/A;C snv 6.8E-05 2.6E-04 0.700 0
Medullary nephrocalcinosis
CUI: C0403477
Disease: Medullary nephrocalcinosis
2 0.925 0.200 3 190408323 missense variant G/A;C snv 6.8E-05 2.6E-04 0.700 0
Polyuria
CUI: C0032617
Disease: Polyuria
3 0.925 0.200 3 190408323 missense variant G/A;C snv 6.8E-05 2.6E-04 0.700 0
Primary hypomagnesemia (disorder)
CUI: C0268448
Disease: Primary hypomagnesemia (disorder)
22 0.925 0.200 3 190408323 missense variant G/A;C snv 6.8E-05 2.6E-04 0.700 0