rs12654812, RGS14

N. diseases: 5
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.
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.925 0.120 5 177367190 intron variant G/A snv 0.34 0.800 1.000 1 2012 2012
Kidney Calculi
CUI: C0022650
Disease: Kidney Calculi
71 0.925 0.120 5 177367190 intron variant G/A snv 0.34 0.740 1.000 5 2013 2019
von Willebrand's factor (lab test)
CUI: C2239219
Disease: von Willebrand's factor (lab test)
427 0.925 0.120 5 177367190 intron variant G/A snv 0.34 0.700 1.000 1 2013 2013
Nephrolithiasis
CUI: C0392525
Disease: Nephrolithiasis
99 0.925 0.120 5 177367190 intron variant G/A snv 0.34 0.040 1.000 4 2013 2019
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.925 0.120 5 177367190 intron variant G/A snv 0.34 0.010 1.000 1 2018 2018