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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001042432.2(CLN3):c.768C>T (p.Thr256=)	rs145967477	0.00103
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.677+8G>A	rs368568189	0.00015
NM_001042432.2(CLN3):c.1209G>A (p.Glu403=)	rs377369610	0.00008
NM_001042432.2(CLN3):c.1210C>A (p.His404Asn)	rs146610181

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