List of variants in gene KIF14 reported as likely benign for Meckel syndrome

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_014875.3(KIF14):c.4842C>T (p.Asp1614=)	rs12024960	0.00284
NM_014875.3(KIF14):c.1087G>A (p.Val363Ile)	rs77828651	0.00249

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