List of variants in gene KANSL1 reported as uncertain significance by Ambry Genetics

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.895C>T (p.Arg299Cys)	rs755353984	0.00001
NM_015443.4(KANSL1):c.1859A>C (p.Asn620Thr)	rs200979425
NM_015443.4(KANSL1):c.2762A>G (p.His921Arg)	rs1555731275

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