List of variants in gene NEK1 reported as likely benign by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_001199397.3(NEK1):c.-488C>T	rs62334514	0.01094
NM_001199397.3(NEK1):c.2235T>G (p.Asn745Lys)	rs34324114	0.00417
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.924T>G (p.Ile308Met)	rs10034957	0.00151
NM_001199397.3(NEK1):c.*1222T>G	rs543801862	0.00028
NM_001199397.3(NEK1):c.-504T>C	rs550632789	0.00017
NM_001199397.3(NEK1):c.1063A>G (p.Arg355Gly)	rs35763578	0.00003
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
NM_001199397.3(NEK1):c.397-15del	rs199717920

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