List of variants in gene CLN3 reported as likely benign by Genome Diagnostics Laboratory, Amsterdam University Medical Center

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001042432.2(CLN3):c.771G>A (p.Glu257=)	rs73533466	0.00372
NM_001042432.2(CLN3):c.831G>A (p.Val277=)	rs1142183	0.00045
NM_001042432.2(CLN3):c.1230G>A (p.Ala410=)	rs201206239	0.00039
NM_001042432.2(CLN3):c.45G>A (p.Glu15=)	rs201824641	0.00022
NM_001042432.2(CLN3):c.677+8G>A	rs368568189	0.00014
NM_001042432.2(CLN3):c.222T>C (p.His74=)	rs201225986	0.00005
NM_001042432.2(CLN3):c.777G>A (p.Pro259=)	rs751443804	0.00001

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