Variants in gene KANSL1 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_015443.4(KANSL1):c.*954C>G	rs150500194	0.00393
NM_015443.4(KANSL1):c.2725-7A>G	rs186818985	0.00024
NM_015443.4(KANSL1):c.1157G>T (p.Ser386Ile)	rs143589497	0.00007
NM_015443.4(KANSL1):c.1277G>A (p.Arg426His)	rs764291274	0.00006
NM_015443.4(KANSL1):c.1276C>T (p.Arg426Cys)	rs757224600	0.00005
NM_015443.4(KANSL1):c.1652C>T (p.Thr551Ile)	rs778178483	0.00004
NM_015443.4(KANSL1):c.112G>A (p.Gly38Ser)	rs770738115	0.00002
NM_015443.4(KANSL1):c.2194A>G (p.Thr732Ala)	rs1036089094	0.00001
NM_015443.4(KANSL1):c.2860C>T (p.Arg954Trp)	rs1322831151	0.00001
NM_015443.4(KANSL1):c.2861G>A (p.Arg954Gln)	rs376635152	0.00001
NM_015443.4(KANSL1):c.3019C>T (p.Arg1007Trp)	rs1057522661	0.00001
NM_015443.4(KANSL1):c.682A>T (p.Thr228Ser)	rs762022186	0.00001
NM_015443.4(KANSL1):c.2233A>G (p.Arg745Gly)	rs796052596

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