List of variants in gene CLN6 reported as benign by Illumina Laboratory Services, Illumina

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_017882.2(CLN6):c.*1157A>G	rs8028241	0.58511
NM_017882.3(CLN6):c.*817C>T	rs8142	0.51081
NM_017882.3(CLN6):c.*1015T>C	rs6494720	0.07280
NM_017882.3(CLN6):c.*690A>G	rs8033190	0.07262
NM_017882.3(CLN6):c.*667G>A	rs111879561	0.00596
NM_017882.3(CLN6):c.298-6C>T	rs117038427	0.00549
NM_017882.3(CLN6):c.214G>C (p.Glu72Gln)	rs104894483	0.00140
NM_017882.3(CLN6):c.*725C>T	rs369225795	0.00002
NM_017882.2(CLN6):c.-178_-169delTCCGCTCCGC	rs55672378
NM_017882.3(CLN6):c.*141GT[11]	rs3837692

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