List of variants in gene COL11A2 reported as likely benign for nonsyndromic genetic hearing loss

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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
NM_080680.3(COL11A2):c.2186G>A (p.Arg729Gln)	rs61730262	0.00339
NM_080680.3(COL11A2):c.4230+13C>G	rs200051654	0.00019
NM_080680.3(COL11A2):c.4587G>A (p.Pro1529=)	rs765931315	0.00010
NM_080680.3(COL11A2):c.2737-4C>T	rs1322401943	0.00004

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