Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10889332
rs10889332
DOCK7
1.000 0.120 1 62485187 3 prime UTR variant C/T snv 0.39
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0.700 1.000 1 2012 2012
dbSNP: rs10889332
rs10889332
DOCK7
1.000 0.120 1 62485187 3 prime UTR variant C/T snv 0.39
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10889332
rs10889332
DOCK7
1.000 0.120 1 62485187 3 prime UTR variant C/T snv 0.39
CUI: C0410529
Disease: Hypochondroplasia (disorder)
Hypochondroplasia (disorder) 		0.010 1.000 1 2016 2016
dbSNP: rs10889332
rs10889332
DOCK7
1.000 0.120 1 62485187 3 prime UTR variant C/T snv 0.39
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.010 1.000 1 2016 2016