Variants in gene CLN3 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001042432.2(CLN3):c.*99C>T	rs113845299	0.00853
NM_001042432.2(CLN3):c.-129G>C	rs141305257	0.00315
NM_001042432.2(CLN3):c.768C>T (p.Thr256=)	rs145967477	0.00103
NM_001042432.1(CLN3):c.-264C>G	rs187163584	0.00096
NM_001042432.2(CLN3):c.238A>T (p.Thr80Ser)	rs150348015	0.00074
NM_001042432.2(CLN3):c.831G>A (p.Val277=)	rs1142183	0.00045
NM_001042432.2(CLN3):c.1230G>A (p.Ala410=)	rs201206239	0.00040
NM_001042432.2(CLN3):c.242C>T (p.Pro81Leu)	rs137906617	0.00029
NM_001042432.2(CLN3):c.677+8G>A	rs368568189	0.00015
NM_001042432.2(CLN3):c.291G>A (p.Thr97=)	rs367945307	0.00007
NM_001042432.2(CLN3):c.1158C>T (p.Gly386=)	rs145340637	0.00005
NM_001042432.2(CLN3):c.*29A>G	rs778438984	0.00004
NM_001042432.2(CLN3):c.125+3G>A	rs775577824	0.00004
NM_001042432.2(CLN3):c.516C>T (p.Leu172=)	rs148846795	0.00004
NM_001042432.2(CLN3):c.1198-5C>T	rs764999720	0.00003
NM_001042432.2(CLN3):c.1210C>A (p.His404Asn)	rs146610181
NM_001042432.2(CLN3):c.537C>G (p.Ala179=)	rs147667964

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