List of variants reported as likely pathogenic for hypertensive disorder by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000092.5(COL4A4):c.2320G>C (p.Gly774Arg)	rs569681869	0.00004
NM_000092.5(COL4A4):c.4394G>A (p.Gly1465Asp)	rs533297350	0.00004
NM_001009944.3(PKD1):c.11524T>C (p.Trp3842Arg)	rs1057518959
NM_001009944.3(PKD1):c.9185T>A (p.Val3062Asp)	rs1057518856
NM_002473.6(MYH9):c.4271A>G (p.Asp1424Gly)	rs867593888
NM_022455.5(NSD1):c.6050G>A (p.Arg2017Gln)	rs587784177
NM_022489.4(INF2):c.658G>A (p.Glu220Lys)	rs530391015

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