List of variants reported as likely pathogenic for hypertensive disorder by Center for Personalized Medicine, Children's Hospital Los Angeles

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001089.3(ABCA3):c.875A>T (p.Glu292Val)	rs149989682	0.00304
NM_004004.6(GJB2):c.488T>C (p.Met163Thr)	rs1273330603	0.00003
NM_001270974.2(HYDIN):c.10816G>T (p.Gly3606Ter)	rs1567744830

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