List of variants in gene CEACAM16 reported as pathogenic for autosomal dominant nonsyndromic hearing loss 4B

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001039213.4(CEACAM16):c.763A>G (p.Arg255Gly)	rs1347137461	0.00001
NM_001039213.4(CEACAM16):c.418A>C (p.Thr140Pro)	rs387907149
NM_001039213.4(CEACAM16):c.505G>A (p.Gly169Arg)	rs876661405

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