List of variants in gene COL9A2 reported as likely benign for retinal disorder

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001852.4(COL9A2):c.1323+18T>G	rs186166446	0.00363
NM_001852.4(COL9A2):c.1237C>T (p.Pro413Ser)	rs201985170	0.00009
NM_001852.4(COL9A2):c.1871-8G>T	rs372902486	0.00006

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