Variants in gene ERCC4 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 5

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HGVS	dbSNP	gnomAD frequency
NM_005236.3(ERCC4):c.1135C>T (p.Pro379Ser)	rs1799802	0.00471
NM_005236.3(ERCC4):c.2117T>C (p.Ile706Thr)	rs1800069	0.00190
NM_005236.3(ERCC4):c.1563C>G (p.Ser521Arg)	rs41552412	0.00099
NM_005236.3(ERCC4):c.211T>C (p.Tyr71His)	rs145315496	0.00027
NM_005236.3(ERCC4):c.973+11A>T	rs185779788	0.00013

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