Variants in gene NEBL with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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_006393.3(NEBL):c.180G>C (p.Lys60Asn)	rs41277374	0.00382
NM_006393.3(NEBL):c.480+3A>G	rs71578983	0.00336
NM_006393.3(NEBL):c.604G>A (p.Gly202Arg)	rs137973321	0.00210
NM_006393.3(NEBL):c.267C>G (p.Tyr89Ter)	rs147622517	0.00154
NM_006393.3(NEBL):c.2346+6G>A	rs201822024	0.00006

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