List of variants in gene COL11A2 reported as likely pathogenic for Rare genetic deafness

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_080680.3(COL11A2):c.3100C>T (p.Arg1034Cys)	rs121912947
NM_080680.3(COL11A2):c.3116G>T (p.Gly1039Val)	rs1554216943
NM_080680.3(COL11A2):c.4943A>T (p.His1648Leu)	rs1487325262

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