Disease: Hypertensive disease ×
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: rs2241766
rs2241766 		0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.080 0.750 8 2006 2019
dbSNP: rs1501299
rs1501299 		0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.050 0.800 5 2011 2019
dbSNP: rs266729
rs266729 		0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.040 1.000 4 2010 2017
dbSNP: rs185847354
rs185847354 		0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2004 2004