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

Submission 1 (benign) minimum review status:		Submission 1 (benign) 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001199397.3(NEK1):c.1388C>T (p.Ala463Val)	rs34540355	0.03694
NM_001199397.3(NEK1):c.3624T>C (p.Asp1208=)	rs55740606	0.00560
NM_001199397.3(NEK1):c.2731C>G (p.Gln911Glu)	rs6828134	0.00535
NM_001199397.3(NEK1):c.2235T>G (p.Asn745Lys)	rs34324114	0.00417
NM_001199397.3(NEK1):c.3285C>T (p.Pro1095=)	rs140408058	0.00301
NM_001199397.3(NEK1):c.975A>G (p.Gly325=)	rs150904906	0.00218
NM_001199397.3(NEK1):c.782G>A (p.Arg261His)	rs200161705	0.00216
NM_001199397.3(NEK1):c.1581T>C (p.Ala527=)	rs184804243	0.00188
NM_001199397.3(NEK1):c.3411G>A (p.Leu1137=)	rs56077602	0.00169
NM_001199397.3(NEK1):c.3213C>T (p.Asn1071=)	rs184324310	0.00098
NM_001199397.3(NEK1):c.2137G>A (p.Val713Met)	rs199827465	0.00063
NM_001199397.3(NEK1):c.2093T>C (p.Met698Thr)	rs577165880	0.00001
NM_001199397.3(NEK1):c.2726C>G (p.Ser909Cys)	rs543224510	0.00001
NM_001199397.3(NEK1):c.1081-8dup	rs398124255

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