List of variants in gene LIG1 reported as uncertain significance for immune system disorder

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000234.3(LIG1):c.2014C>T (p.Arg672Cys)	rs55950593	0.00026
NM_000234.3(LIG1):c.1331+6C>T	rs370406559	0.00021
NM_000234.3(LIG1):c.778C>T (p.Pro260Ser)	rs759755473	0.00012
NM_000234.3(LIG1):c.2311C>T (p.Arg771Trp)	rs121434561	0.00001
NM_000234.3(LIG1):c.1306del (p.His436fs)
NM_000234.3(LIG1):c.191T>C (p.Leu64Pro)
NM_000234.3(LIG1):c.2326G>A (p.Gly776Arg)
NM_000234.3(LIG1):c.97C>A (p.Pro33Thr)

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