List of variants reported as uncertain significance for hypertensive disorder by Johns Hopkins Genomics, Johns Hopkins University

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000352.6(ABCC8):c.2539G>A (p.Ala847Thr)	rs561593131
NM_001127217.3(SMAD9):c.205G>A (p.Val69Ile)
NM_001204.7(BMPR2):c.1250T>G (p.Phe417Cys)
NM_001204.7(BMPR2):c.2362G>A (p.Val788Ile)
NM_002246.3(KCNK3):c.172G>A (p.Gly58Ser)	rs753384871

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