List of variants in gene KIF22 reported as likely pathogenic for bone development disease

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_007317.3(KIF22):c.1399G>A (p.Glu467Lys)	rs1596854441
NM_007317.3(KIF22):c.443C>T (p.Pro148Leu)	rs193922921
NM_007317.3(KIF22):c.752T>C (p.Leu251Pro)	rs2142373200

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