List of variants in gene KIF14 reported as likely pathogenic for Microcephaly 20, primary, autosomal recessive

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: 4

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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.14G>T (p.Ser5Ile)	rs1256629719
NM_014875.3(KIF14):c.2813+2dup
NM_014875.3(KIF14):c.4071G>A (p.Gln1357=)	rs1553254322

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