List of variants reported as pathogenic for Norum disease by Fulgent Genetics, Fulgent Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000229.2(LCAT):c.321C>A (p.Tyr107Ter)	rs121908055	0.00004
NM_000229.2(LCAT):c.440C>T (p.Thr147Ile)	rs121908050	0.00004
NM_000229.2(LCAT):c.101C>T (p.Pro34Leu)	rs121908051
NM_000229.2(LCAT):c.511C>T (p.Arg171Trp)

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