Variants in gene KANSL1 with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 4

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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.1774C>T (p.Arg592Trp)	rs774841964
NM_015443.4(KANSL1):c.3031C>T (p.Arg1011Ter)	rs779686052

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