List of variants in gene CLN3 reported as benign for not provided

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_001042432.2(CLN3):c.294+236A>G	rs149282	0.98043
NM_001042432.2(CLN3):c.294+265A>T	rs149281	0.93847
NM_001042432.2(CLN3):c.1057-148A>G	rs34839	0.48008
NM_001042432.2(CLN3):c.295-229T>C	rs34835	0.36719
NM_001042432.2(CLN3):c.1057-144C>T	rs28374519	0.33844
NM_001042432.2(CLN3):c.678-313G>A	rs151182	0.31813
NM_001042432.2(CLN3):c.294+253T>A	rs149301	0.29597
NM_001042432.2(CLN3):c.1211A>G (p.His404Arg)	rs77595156	0.11421
NM_001042432.2(CLN3):c.-77+85G>A	rs28612835	0.04930
NM_001042432.2(CLN3):c.46+63A>G	rs28545628	0.04650
NM_001042432.2(CLN3):c.1056+140G>A	rs143833407	0.02751
NC_000016.10:g.28492377T>C	rs867543183	0.02499
NM_001042432.2(CLN3):c.295-59G>A	rs79077329	0.02245
NM_001042432.2(CLN3):c.47-60C>G	rs111404007	0.01636
NM_001042432.2(CLN3):c.677+147C>G	rs56695328	0.01496
NM_001042432.2(CLN3):c.1057-55C>T	rs74016815	0.01495
NM_001042432.2(CLN3):c.771G>A (p.Glu257=)	rs73533466	0.00402
NM_001042432.2(CLN3):c.768C>T (p.Thr256=)	rs145967477	0.00103
NM_001042432.2(CLN3):c.1209G>A (p.Glu403=)	rs377369610	0.00008
NM_001042432.2(CLN3):c.240G>A (p.Thr80=)	rs373911322	0.00002
NC_000016.10:g.28492317_28492322del	rs72224211
NC_000016.10:g.28492396del	rs764760757
NC_000016.10:g.28492396dup	rs764760757
NM_001042432.2(CLN3):c.1056+102dup	rs371817940
NM_001042432.2(CLN3):c.1057-22dup	rs148146139
NM_001042432.2(CLN3):c.294+266_294+267del	rs367752281
NM_001042432.2(CLN3):c.414C>T (p.Ser138=)	rs772960606
NM_001042432.2(CLN3):c.790+281_790+292del	rs755660742
NM_001042432.2(CLN3):c.790+292del	rs755660742

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