rs784257, LOC105372130

N. diseases: 4
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.
Albuminuria
CUI: C0001925
Disease: Albuminuria
59 1.000 0.080 18 55729968 intron variant T/A;C snv 0.700 1.000 1 2018 2018
Fuchs Endothelial Dystrophy
CUI: C0016781
Disease: Fuchs Endothelial Dystrophy
32 1.000 0.080 18 55729968 intron variant T/A;C snv 0.700 1.000 1 2017 2017
Potassium measurement
CUI: C0202194
Disease: Potassium measurement
28 1.000 0.080 18 55729968 intron variant T/A;C snv 0.700 1.000 1 2019 2019
Sodium measurement
CUI: C0337443
Disease: Sodium measurement
69 1.000 0.080 18 55729968 intron variant T/A;C snv 0.700 1.000 1 2019 2019