Table 3.

Association Analyses

	SNP	CHR	Gene	Functional Consequence
SBP	rs1630736	6	EDN1	intron variant
	rs1902859	4	FGF5 (nearby)	n/a
	rs2076283	1	ECE1	intron variant
	rs212544	1	ECE1	intron variant
	rs2236847	1	ECE1	intron variant
	rs2336384	1	MFN2	intron variant
	rs2774028	1	ECE1	intron variant
	rs3827750	1	AGT	intron variant
	rs4409766	10	BORCS7	intron variant
	rs4980974	3	AGTR1	intron variant
	rs5193	X	AGTR2	utr variant 3 prime
	rs5370	6	EDN1	missense
	rs6632677	X	ACE2	intron variant
	rs7305099	12	WNK1	intron variant
DBP	rs11122575	1	AGT	intron variant
	rs11608756	12	WNK1	intron variant
	rs1902859	4	FGF5 (nearby)	n/a
	rs2074192	X	ACE2	intron variant
	rs2106809	X	ACE2	intron variant
	rs212544	1	ECE1	intron variant
	rs2493132	1	AGT	intron variant
	rs3827750	1	AGT	intron variant
	rs3889728	1	AGT	intron variant
	rs4340	17	ACE	287 bp pathogenic indel
	rs5193	X	AGTR2	utr variant 3 prime
	rs5370	6	EDN1	missense
	rs7305099	12	WNK1	intron variant

SNP: single nucleotide polymorphism; CHR: chromosome; SBP: systolic blood pressure; DBP: diastolic blood pressure.