Variants in gene ELN with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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_000501.4(ELN):c.1150+1G>A	rs727503030	0.00005
NM_000501.4(ELN):c.1733del (p.Pro578fs)	rs727503782
NM_000501.4(ELN):c.1858G>T (p.Gly620Ter)	rs727503034
NM_000501.4(ELN):c.2T>C (p.Met1Thr)	rs863223518
NM_000501.4(ELN):c.643+1G>A	rs1131691482

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