List of variants in gene KIF5C reported as uncertain significance for Inborn genetic diseases

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_004522.3(KIF5C):c.88A>G (p.Ile30Val)	rs201371161	0.00005
NM_004522.3(KIF5C):c.10C>T (p.Pro4Ser)
NM_004522.3(KIF5C):c.124G>C (p.Gly42Arg)
NM_004522.3(KIF5C):c.79G>A (p.Asp27Asn)	rs916435347

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