List of variants reported as risk factor for Hyperlipidemia, familial combined, susceptibility to

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_007122.5(USF1):c.561-100G>A	rs2073658	0.21615
NM_007122.5(USF1):c.*187C>T	rs3737787	0.21525
NM_000237.2(LPL):c.-281T>G	rs1800590	0.12919
NM_000237.3(LPL):c.106G>A (p.Asp36Asn)	rs1801177	0.01951
NM_000237.3(LPL):c.953A>G (p.Asn318Ser)	rs268	0.01327
NC_000008.11:g.19939214T>C	rs2128835067

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