List of variants in gene COG1 reported as likely benign by GeneDx

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
NC_000017.11:g.73192846C>G	rs8076009	0.25989
NM_018714.3(COG1):c.2729+28G>A	rs143165734	0.00108
NM_018714.3(COG1):c.2805+39C>T	rs186737076	0.00097
NC_000017.11:g.73192832_73192883del	rs1568292927

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