List of variants in gene CEACAM16 reported as uncertain significance for auditory system disease

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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: 7

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HGVS	dbSNP
NM_001039213.4(CEACAM16):c.-8G>A
NM_001039213.4(CEACAM16):c.1054C>T (p.Arg352Cys)
NM_001039213.4(CEACAM16):c.1135C>T (p.Arg379Trp)
NM_001039213.4(CEACAM16):c.220G>A (p.Asp74Asn)
NM_001039213.4(CEACAM16):c.245C>T (p.Thr82Met)
NM_001039213.4(CEACAM16):c.520G>A (p.Ala174Thr)	rs750153629
NM_001039213.4(CEACAM16):c.565C>T (p.His189Tyr)	rs370890913

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