List of variants in gene KANSL1 reported as likely pathogenic 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_015443.4(KANSL1):c.868C>T (p.Arg290Ter)	rs149830411	0.00006
NM_015443.4(KANSL1):c.808_809del (p.Leu270fs)	rs551541795	0.00001
NM_015443.4(KANSL1):c.2837+1G>A	rs2077054270

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