List of variants reported as benign for familial apolipoprotein C-II deficiency

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000483.4(APOC2):c.-62T>G	rs2288911	0.59500
NM_000483.5(APOC2):c.188_189insT	rs150448996	0.28355
NM_000483.5(APOC2):c.*306C>T	rs1130742	0.28341
NM_000483.5(APOC2):c.*90C>T	rs7253690	0.01361
NM_000483.5(APOC2):c.56-4G>C	rs74500990	0.01248
NM_000483.5(APOC2):c.229A>C (p.Lys77Gln)	rs5126	0.00784
NM_000483.5(APOC2):c.-2C>T	rs5121	0.00686
NM_000483.5(APOC2):c.122A>C (p.Lys41Thr)	rs120074114	0.00071

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