rs2731672, GRK6

N. diseases: 6
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.
Activated Partial Thromboplastin Time measurement
CUI: C0030605
Disease: Activated Partial Thromboplastin Time measurement
44 5 177415473 intron variant T/C snv 0.66 0.800 1.000 1 2010 2010
Amino acids measurement
CUI: C0201874
Disease: Amino acids measurement
92 5 177415473 intron variant T/C snv 0.66 0.700 1.000 1 2016 2016
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
205 5 177415473 intron variant T/C snv 0.66 0.700 1.000 1 2012 2012
Protein measurement
CUI: C0202202
Disease: Protein measurement
422 5 177415473 intron variant T/C snv 0.66 0.700 1.000 1 2016 2016
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 5 177415473 intron variant T/C snv 0.66 0.700 1.000 1 2012 2012
von Willebrand's factor (lab test)
CUI: C2239219
Disease: von Willebrand's factor (lab test)
427 5 177415473 intron variant T/C snv 0.66 0.700 1.000 1 2013 2013