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

Submission 1 (benign) minimum review status:		Submission 1 (benign) 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: 26

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HGVS	dbSNP	gnomAD frequency
NM_015443.4(KANSL1):c.2109A>G (p.Leu703=)	rs34101027	0.00967
NM_015443.4(KANSL1):c.773T>C (p.Leu258Ser)	rs145714368	0.00328
NM_015443.4(KANSL1):c.727C>A (p.Gln243Lys)	rs142096969	0.00174
NM_015443.4(KANSL1):c.1653-10C>G	rs199642265	0.00170
NM_015443.4(KANSL1):c.1826G>A (p.Ser609Asn)	rs138698439	0.00157
NM_015443.4(KANSL1):c.607G>C (p.Gly203Arg)	rs138175526	0.00156
NM_015443.4(KANSL1):c.1116A>G (p.Lys372=)	rs62639965	0.00107
NM_015443.4(KANSL1):c.2628C>T (p.Arg876=)	rs149756887	0.00087
NM_015443.4(KANSL1):c.1938C>T (p.Pro646=)	rs371047711	0.00070
NM_015443.4(KANSL1):c.2481C>T (p.Ser827=)	rs143653891	0.00044
NM_015443.4(KANSL1):c.571G>T (p.Gly191Cys)	rs149566146	0.00042
NM_015443.4(KANSL1):c.635A>G (p.His212Arg)	rs141110759	0.00038
NM_015443.4(KANSL1):c.2294C>T (p.Ala765Val)	rs151099014	0.00036
NM_015443.4(KANSL1):c.2698G>A (p.Gly900Arg)	rs74867664	0.00032
NM_015443.4(KANSL1):c.2725-7A>G	rs186818985	0.00024
NM_015443.4(KANSL1):c.286T>C (p.Leu96=)	rs140268765	0.00024
NM_015443.4(KANSL1):c.620A>G (p.Asn207Ser)	rs144882998	0.00019
NM_015443.4(KANSL1):c.2110T>C (p.Ser704Pro)	rs202231419	0.00015
NM_015443.4(KANSL1):c.3053C>T (p.Thr1018Ile)	rs145863194	0.00006
NM_015443.4(KANSL1):c.3306G>A (p.Pro1102=)	rs143746890	0.00006
NM_015443.4(KANSL1):c.729A>G (p.Gln243=)	rs775976415	0.00006
NM_015443.4(KANSL1):c.2414T>C (p.Met805Thr)	rs201526313	0.00004
NM_015443.4(KANSL1):c.1855C>T (p.Arg619Trp)	rs141298741	0.00003
NM_015443.4(KANSL1):c.1857G>T (p.Arg619=)	rs191986791
NM_015443.4(KANSL1):c.2710GAG[1] (p.Glu905del)	rs551968687
NM_015443.4(KANSL1):c.680G>A (p.Ser227Asn)	rs150345690

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