AGT, angiotensinogen, 183

N. diseases: 765; N. variants: 43
Disease: Essential Hypertension ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs699
rs699 		0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		Cardiovascular Diseases 0.100 0.795 39 1993 2014
dbSNP: rs4762
rs4762 		0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		Cardiovascular Diseases 0.090 0.667 9 1994 2015
dbSNP: rs2478544
rs2478544 		1.000 0.040 1 230708450 intron variant C/A;G;T snv
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		Cardiovascular Diseases 0.010 1.000 1 2015 2015