List of variants reported as uncertain significance for atrial septal defect 4 by Fulgent Genetics, Fulgent Genetics

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001077653.2(TBX20):c.1309C>T (p.Arg437Cys)	rs200704561	0.00015
NM_001077653.2(TBX20):c.1310G>A (p.Arg437His)	rs375484585	0.00014
NM_001077653.2(TBX20):c.457G>A (p.Val153Ile)	rs776152314	0.00011
NM_001077653.2(TBX20):c.418G>A (p.Val140Met)	rs766745923	0.00009
NM_001077653.2(TBX20):c.599T>C (p.Met200Thr)	rs151183955	0.00006
NM_001077653.2(TBX20):c.86C>G (p.Ser29Cys)	rs13237089	0.00005
NM_001077653.2(TBX20):c.785C>T (p.Thr262Met)	rs747369702	0.00003
NM_001077653.2(TBX20):c.1036C>G (p.Leu346Val)	rs768158277	0.00002
NM_001077653.2(TBX20):c.1046G>C (p.Trp349Ser)	rs748900621	0.00001
NM_001077653.2(TBX20):c.395C>T (p.Thr132Ile)	rs200630726	0.00001
NM_001077653.2(TBX20):c.413C>T (p.Ser138Leu)	rs778902854	0.00001
NM_001077653.2(TBX20):c.456C>G (p.Ile152Met)	rs137852954	0.00001
NM_001077653.2(TBX20):c.4G>A (p.Glu2Lys)	rs752468331	0.00001
NM_001077653.2(TBX20):c.533C>T (p.Pro178Leu)	rs760169368	0.00001
NM_001077653.2(TBX20):c.818C>T (p.Thr273Met)	rs1554286367

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