List of variants reported as likely benign for chromosome 10 disorder by Fulgent Genetics, Fulgent Genetics

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001002295.2(GATA3):c.1050+19G>A	rs150545188	0.00072
NM_001002295.2(GATA3):c.294C>T (p.Asp98=)	rs144221016	0.00039
NM_001002295.2(GATA3):c.375C>T (p.Gly125=)	rs142451494	0.00029
NM_001002295.2(GATA3):c.330C>T (p.Ser110=)	rs111978415	0.00027
NM_001002295.2(GATA3):c.591G>A (p.Glu197=)	rs372630189	0.00018
NM_001002295.2(GATA3):c.870C>T (p.Leu290=)	rs575091	0.00007
NM_001002295.2(GATA3):c.359C>T (p.Thr120Met)	rs750735308	0.00003
NM_001002295.2(GATA3):c.948G>A (p.Thr316=)	rs12572959	0.00001
NM_001002295.2(GATA3):c.373_375dup (p.Gly125dup)	rs547425013
NM_001002295.2(GATA3):c.480C>T (p.Asp160=)	rs143627754
NM_001002295.2(GATA3):c.706C>G (p.Pro236Ala)	rs148835259
NM_001002295.2(GATA3):c.724G>A (p.Gly242Ser)	rs11567901
NM_001002295.2(GATA3):c.82C>A (p.His28Asn)
NM_001002295.2(GATA3):c.86C>T (p.Pro29Leu)
NM_001002295.2(GATA3):c.925-7CT[3]

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