Source: BEFREE

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: rs3889728
rs3889728
AGT
1.000 0.120 1 230713085 intron variant C/T snv 0.24
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.020 1.000 2 2015 2019
dbSNP: rs3889728
rs3889728
AGT
1.000 0.120 1 230713085 intron variant C/T snv 0.24
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma 		0.010 1.000 1 2015 2015