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: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.100 0.857 14 1998 2019
dbSNP: rs4762
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.030 0.667 3 1998 2019
dbSNP: rs5050
rs5050
AGT
0.827 0.200 1 230714140 intron variant T/C;G snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.010 1.000 1 2019 2019