List of variants in gene COL11A1 reported as uncertain significance for Hearing impairment

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001854.4(COL11A1):c.2014G>A (p.Asp672Asn)	rs143663917	0.00031
NM_001854.4(COL11A1):c.5359G>A (p.Asp1787Asn)	rs144510951	0.00007
NM_001854.4(COL11A1):c.3779C>A (p.Ala1260Glu)	rs750838060	0.00003
NM_001854.4(COL11A1):c.4700A>G (p.Asp1567Gly)	rs756511227	0.00001
NM_001854.4(COL11A1):c.3472G>T (p.Val1158Phe)	rs2101222310
NM_001854.4(COL11A1):c.4691A>G (p.Asp1564Gly)	rs2100840741

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