rs80356708, GRHPR

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 hyperoxaluria type 2
CUI: C0268165
Disease: Primary hyperoxaluria type 2
55 0.882 0.160 9 37424862 frameshift variant G/- delins 0.700 1.000 5 1999 2008
Nephrocalcinosis
CUI: C0027709
Disease: Nephrocalcinosis
20 0.882 0.160 9 37424862 frameshift variant G/- delins 0.700 1.000 1 2018 2018
Nephrolithiasis
CUI: C0392525
Disease: Nephrolithiasis
99 0.882 0.160 9 37424862 frameshift variant G/- delins 0.700 1.000 1 2018 2018