List of variants reported as likely benign for syndromic dyslipidemia by Pars Genome Lab

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000404.4(GLB1):c.734-80G>A	rs75639377	0.05351
NM_001360.3(DHCR7):c.399C>T (p.Ala133=)	rs147424205	0.00248
NM_000404.4(GLB1):c.1233+91G>C	rs2125474421
NM_000404.4(GLB1):c.733+78A>G	rs77452319

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