List of variants reported as likely benign for syndromic dyslipidemia by Counsyl

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000404.4(GLB1):c.1306C>T (p.Leu436Phe)	rs34421970	0.00952
NM_000404.4(GLB1):c.858C>T (p.Thr286=)	rs770638519	0.00002
NM_000235.4(LIPA):c.1188G>A (p.Arg396=)	rs750001661	0.00001
NM_000784.4(CYP27A1):c.882G>A (p.Glu294=)	rs59428328	0.00001
NM_000288.4(PEX7):c.130+32_130+51del	rs1554328334
NM_000382.3(ALDH3A2):c.1443+1222del
NM_000404.4(GLB1):c.1310A>G (p.Asn437Ser)	rs202237232

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