ClinVar Miner

List of variants in gene COL11A2 studied for Nonsyndromic genetic hearing loss

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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_080680.3(COL11A2):c.889G>A (p.Gly297Ser)	rs139116571	0.00012
NM_080680.3(COL11A2):c.3950T>C (p.Leu1317Pro)	rs145871842	0.00006
NM_080680.3(COL11A2):c.3974C>T (p.Ser1325Leu)	rs543145528	0.00004

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