List of variants in gene KIF14 reported as pathogenic for not provided

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_014875.3(KIF14):c.103C>T (p.Arg35Ter)	rs774318019	0.00001
NM_014875.3(KIF14):c.2362C>T (p.Gln788Ter)
NM_014875.3(KIF14):c.521_522del (p.Phe174fs)

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