Variants in gene NEK1 with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001199397.3(NEK1):c.3107C>G (p.Ser1036Ter)	rs199947197	0.00009
NM_001199397.3(NEK1):c.1226G>A (p.Trp409Ter)	rs985064686	0.00004
NM_001199397.3(NEK1):c.214+1G>A	rs1049502301	0.00002
NM_001199397.3(NEK1):c.1618C>T (p.Arg540Ter)	rs758677637	0.00001
NM_001199397.3(NEK1):c.418G>A (p.Gly140Arg)	rs1301705612	0.00001
NM_001199397.3(NEK1):c.1769_1770del (p.Arg590fs)	rs1554053289
NM_001199397.3(NEK1):c.1868del (p.Ser623fs)	rs1362848762
NM_001199397.3(NEK1):c.2814_2817del (p.Asn938fs)	rs752878896
NM_001199397.3(NEK1):c.2886-1G>A	rs773496891
NM_001199397.3(NEK1):c.599_602del (p.Lys200fs)	rs1554075284

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