List of variants reported as uncertain significance for pulmonary hypertension, primary, 3 by Labcorp Genetics (formerly Invitae), Labcorp

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001753.5(CAV1):c.202T>G (p.Phe68Val)	rs752571940	0.00006
NM_001753.5(CAV1):c.512G>A (p.Arg171His)	rs772468332	0.00004
NM_001753.5(CAV1):c.238A>G (p.Ser80Gly)	rs369884333	0.00001
NM_001753.5(CAV1):c.302G>A (p.Arg101His)	rs200052661	0.00001
NC_000007.13:g.(?_116165117)_(116199341_?)del
NC_000007.13:g.(?_116165117)_(116199341_?)dup
NM_001753.5(CAV1):c.211G>A (p.Val71Met)
NM_001753.5(CAV1):c.229G>A (p.Gly77Arg)
NM_001753.5(CAV1):c.352T>C (p.Tyr118His)
NM_001753.5(CAV1):c.358G>A (p.Ala120Thr)

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