rs1912826, KLKB1

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.
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
205 4 186228386 intron variant G/A;C snv 0.700 1.000 1 2012 2012
Glycine measurement
CUI: C0523677
Disease: Glycine measurement
68 4 186228386 intron variant G/A;C snv 0.700 1.000 1 2019 2019
Polysomnography
CUI: C0162701
Disease: Polysomnography
249 4 186228386 intron variant G/A;C snv 0.700 1.000 1 2012 2012
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 4 186228386 intron variant G/A;C snv 0.700 1.000 1 2012 2012