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

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001039213.4(CEACAM16):c.520G>A (p.Ala174Thr)	rs750153629	0.00020
NM_001039213.4(CEACAM16):c.565C>T (p.His189Tyr)	rs370890913	0.00017
NM_001039213.4(CEACAM16):c.1191C>A (p.Asp397Glu)	rs543881691	0.00011
NM_001039213.4(CEACAM16):c.551G>A (p.Arg184Gln)	rs577629047	0.00004
NM_001039213.4(CEACAM16):c.1135C>T (p.Arg379Trp)	rs771692758	0.00002
NM_001039213.4(CEACAM16):c.220G>A (p.Asp74Asn)	rs536837008	0.00002
NM_001039213.4(CEACAM16):c.1054C>T (p.Arg352Cys)	rs747961516	0.00001
NM_001039213.4(CEACAM16):c.245C>T (p.Thr82Met)	rs776527204	0.00001
NM_001039213.4(CEACAM16):c.-8G>A	rs1355072516

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