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

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: 24

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HGVS	dbSNP	gnomAD frequency
NM_001042432.2(CLN3):c.1211A>G (p.His404Arg)	rs77595156	0.11421
NM_001042432.2(CLN3):c.771G>A (p.Glu257=)	rs73533466	0.00402
NM_001042432.2(CLN3):c.313A>G (p.Ile105Val)	rs11552531	0.00312
NM_001042432.2(CLN3):c.318C>T (p.Leu106=)	rs148248159	0.00115
NM_001042432.2(CLN3):c.768C>T (p.Thr256=)	rs145967477	0.00103
NM_001042432.2(CLN3):c.963-16C>G	rs200023908	0.00051
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.678-18C>A	rs370158185	0.00031
NM_001042432.2(CLN3):c.790+16C>A	rs200731769	0.00023
NM_001042432.2(CLN3):c.45G>A (p.Glu15=)	rs201824641	0.00022
NM_001042432.2(CLN3):c.677+8G>A	rs368568189	0.00015
NM_001042432.2(CLN3):c.174C>T (p.Ala58=)	rs138433617	0.00014
NM_001042432.2(CLN3):c.1197+13C>T	rs370103287	0.00006
NM_001042432.2(CLN3):c.222T>C (p.His74=)	rs201225986	0.00006
NM_001042432.2(CLN3):c.975G>A (p.Leu325=)	rs150174473	0.00005
NM_001042432.2(CLN3):c.264A>C (p.Ser88=)	rs751321507	0.00004
NM_001042432.2(CLN3):c.295-17C>T	rs375311626	0.00004
NM_001042432.2(CLN3):c.516C>T (p.Leu172=)	rs148846795	0.00004
NM_001042432.2(CLN3):c.240G>A (p.Thr80=)	rs373911322	0.00002
NM_001042432.2(CLN3):c.-76-4G>T	rs796052334	0.00001
NM_001042432.2(CLN3):c.1197+8T>C	rs587780895
NM_001042432.2(CLN3):c.1210C>A (p.His404Asn)	rs146610181
NM_001042432.2(CLN3):c.270T>C (p.Phe90=)	rs145520962

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