List of variants reported as uncertain significance for endocardium disorder

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000116.5(TAFAZZIN):c.*618A>G	rs781924638	0.00007
NM_000116.5(TAFAZZIN):c.*33G>A	rs782129745	0.00002
NM_000116.5(TAFAZZIN):c.351G>A (p.Lys117=)	rs782564325	0.00002
NM_000116.5(TAFAZZIN):c.535C>G (p.Pro179Ala)	rs397515744	0.00001
NM_000116.5(TAFAZZIN):c.*165T>A	rs2068620449
NM_000116.5(TAFAZZIN):c.*387C>T	rs1057515819
NM_000116.5(TAFAZZIN):c.*648A>C	rs1413243483
NM_000116.5(TAFAZZIN):c.49T>C (p.Trp17Arg)	rs2068313278
NM_000116.5(TAFAZZIN):c.504G>A (p.Lys168=)	rs1057515818
NM_000116.5(TAFAZZIN):c.647-6C>T	rs901353067

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