List of variants in gene LIG3 reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_013975.4(LIG3):c.2796+20C>T	rs778468086	0.00004
NM_013975.4(LIG3):c.446G>A (p.Arg149Gln)	rs772050625	0.00002
NM_013975.4(LIG3):c.1193A>G (p.Gln398Arg)	rs781367751	0.00001
NM_013975.4(LIG3):c.1555A>G (p.Asn519Asp)	rs763624496	0.00001
NM_013975.4(LIG3):c.1073T>C (p.Phe358Ser)
NM_013975.4(LIG3):c.1166A>G (p.Lys389Arg)
NM_013975.4(LIG3):c.1690A>C (p.Ile564Leu)	rs1555556264
NM_013975.4(LIG3):c.1824-13C>T
NM_013975.4(LIG3):c.1859A>G (p.Asn620Ser)
NM_013975.4(LIG3):c.2200G>C (p.Asp734His)	rs1567693216
NM_013975.4(LIG3):c.2332-19G>C
NM_013975.4(LIG3):c.2860C>A (p.Arg954Ser)
NM_013975.4(LIG3):c.3023C>T (p.Pro1008Leu)	rs1319167353
NM_013975.4(LIG3):c.382T>G (p.Ser128Ala)	rs1021764612
NM_013975.4(LIG3):c.744T>A (p.Ser248Arg)

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