List of variants reported as uncertain significance for hypertensive disorder by Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001127217.3(SMAD9):c.136AAG[5] (p.Lys49dup)	rs751217637
NM_001127217.3(SMAD9):c.995T>C (p.Ile332Thr)
NM_001321120.2(TBX4):c.557T>G (p.Leu186Arg)	rs886041115

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