List of variants in gene CLN3 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001042432.2(CLN3):c.242C>T (p.Pro81Leu)	rs137906617	0.00029
NM_001042432.2(CLN3):c.206C>T (p.Ser69Leu)	rs769840061	0.00004
NM_001042432.2(CLN3):c.125+3G>A	rs775577824	0.00003
NM_001042432.2(CLN3):c.461-3C>A	rs181995380	0.00003
NM_001042432.2(CLN3):c.266G>A (p.Arg89Gln)	rs766287694	0.00001
NM_001042432.2(CLN3):c.575G>A (p.Gly192Glu)	rs386833733

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