List of variants in gene LIG4 reported as benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_206937.2(LIG4):c.26C>T (p.Thr9Ile)	rs1805388	0.16468
NM_206937.2(LIG4):c.-28-294C>T	rs3093759	0.14452
NM_206937.2(LIG4):c.1704T>C (p.Asp568=)	rs1805386	0.13864
NM_206937.2(LIG4):c.8C>T (p.Ala3Val)	rs1805389	0.04996
NM_206937.2(LIG4):c.-28-37T>C	rs1805384	0.03664
NM_206937.2(LIG4):c.807C>T (p.Tyr269=)	rs2232638	0.03276
NM_206937.2(LIG4):c.*204A>G	rs3093769	0.03275
NM_206937.2(LIG4):c.*131A>T	rs3093768	0.03272
NM_206937.2(LIG4):c.2569G>A (p.Ala857Thr)	rs2232642	0.03272
NM_206937.2(LIG4):c.-7C>T	rs4987182	0.03244
NM_206937.2(LIG4):c.*129A>G	rs3093767	0.02174
NM_206937.2(LIG4):c.513T>C (p.Leu171=)	rs3093764	0.00779
NM_206937.2(LIG4):c.*3del	rs551263548	0.00602
NM_206937.2(LIG4):c.1798G>A (p.Glu600Lys)	rs61731910	0.00599
NM_206937.2(LIG4):c.915T>C (p.Ser305=)	rs2232639	0.00524
NM_206937.2(LIG4):c.-28-123dup	rs3093761

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