List of variants reported as likely benign for syndromic dyslipidemia by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000382.3(ALDH3A2):c.1270C>T (p.Pro424Ser)	rs61737992	0.00419
NM_001166114.2(PNPLA6):c.2359G>A (p.Val787Met)	rs145988230	0.00160
NM_000784.4(CYP27A1):c.1419C>T (p.Val473=)	rs138596741	0.00037
NM_000784.4(CYP27A1):c.789C>T (p.Pro263=)	rs143600636	0.00019
NM_000784.4(CYP27A1):c.432T>C (p.Tyr144=)	rs1553616026	0.00001
NM_000784.4(CYP27A1):c.1471G>T (p.Ala491Ser)	rs72551323

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