List of variants in gene CLN3 reported as uncertain significance by Counsyl

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001042432.2(CLN3):c.1256G>A (p.Gly419Glu)	rs796052338	0.00001
NM_001042432.2(CLN3):c.837+5G>A	rs756848924	0.00001
NM_001042432.2(CLN3):c.725AAG[2] (p.Glu244del)	rs796052340
NM_001042432.2(CLN3):c.853A>G (p.Ile285Val)	rs748844685

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