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

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (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: 22

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HGVS	dbSNP	gnomAD frequency
NM_000501.4(ELN):c.2086+5G>C	rs111866046	0.02303
NM_000501.4(ELN):c.427+8C>T	rs55868272	0.01032
NM_000501.4(ELN):c.1622-13C>T	rs41362346	0.00728
NM_000501.4(ELN):c.892G>A (p.Val298Ile)	rs41526244	0.00347
NM_000501.4(ELN):c.2132G>A (p.Gly711Asp)	rs41511151	0.00318
NM_000501.4(ELN):c.1828G>A (p.Gly610Ser)	rs140425210	0.00288
NM_000501.4(ELN):c.1566T>A (p.Gly522=)	rs61734584	0.00283
NM_000501.4(ELN):c.259T>C (p.Phe87Leu)	rs140411170	0.00080
NM_000501.4(ELN):c.1232T>G (p.Val411Gly)	rs200180992	0.00073
NM_000501.4(ELN):c.212C>T (p.Ala71Val)	rs41350445	0.00073
NM_000501.4(ELN):c.470-10C>G	rs200663056	0.00053
NM_000501.4(ELN):c.366A>G (p.Gly122=)	rs61734587	0.00034
NM_000501.4(ELN):c.1999C>T (p.Pro667Ser)	rs142316834	0.00031
NM_000501.4(ELN):c.1467C>T (p.Val489=)	rs200512332	0.00017
NM_000501.4(ELN):c.232+3G>A	rs377172364	0.00015
NM_000501.4(ELN):c.886G>A (p.Ala296Thr)	rs782335529	0.00006
NM_000501.4(ELN):c.2132-5T>A	rs539160518	0.00004
NM_000501.4(ELN):c.1264G>A (p.Gly422Ser)	rs2071307
NM_000501.4(ELN):c.1269C>T (p.Val423=)	rs61734583
NM_000501.4(ELN):c.133+16C>A	rs144223231
NM_000501.4(ELN):c.134-5C>A	rs202142516
NM_000501.4(ELN):c.1741G>C (p.Gly581Arg)	rs17855988

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