List of variants in gene KIF21A 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001173464.2(KIF21A):c.*71C>G	rs111409014	0.00191
NM_001173464.2(KIF21A):c.1542G>A (p.Ala514=)	rs199973182	0.00021
NM_001173464.2(KIF21A):c.162A>G (p.Val54=)	rs754537818	0.00011
NM_001173464.2(KIF21A):c.1851G>A (p.Glu617=)	rs147473938	0.00008
NM_001173464.2(KIF21A):c.3320-4A>T	rs371915160	0.00006
NM_001173464.2(KIF21A):c.4277C>T (p.Thr1426Met)	rs781214904	0.00006
NM_001173464.2(KIF21A):c.568G>A (p.Val190Ile)	rs141530856	0.00003
NM_001173464.2(KIF21A):c.2492C>T (p.Thr831Met)	rs764601859
NM_001173464.2(KIF21A):c.3341-11dup	rs71075059

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