List of variants reported as likely pathogenic for syndromic dyslipidemia by Genome-Nilou Lab

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000237.3(LPL):c.347G>A (p.Arg116Gln)	rs775728208	0.00002
NM_000784.4(CYP27A1):c.1415G>C (p.Gly472Ala)	rs200883871	0.00001

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