rs779588655, SLC12A1

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.
Nephrocalcinosis
CUI: C0027709
Disease: Nephrocalcinosis
20 0.882 0.160 15 48234946 frameshift variant T/- delins 8.0E-06 0.700 1.000 1 2018 2018
Nephrolithiasis
CUI: C0392525
Disease: Nephrolithiasis
99 0.882 0.160 15 48234946 frameshift variant T/- delins 8.0E-06 0.700 1.000 1 2018 2018
Bartter syndrome, antenatal type 1
CUI: C1866495
Disease: Bartter syndrome, antenatal type 1
15 0.882 0.160 15 48234946 frameshift variant T/- delins 8.0E-06 0.700 0