List of variants in gene CEACAM16 reported as likely pathogenic for perceptual disorders

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001039213.4(CEACAM16):c.1097C>T (p.Pro366Leu)	rs762367899	0.00001
NM_001039213.4(CEACAM16):c.1057G>A (p.Gly353Arg)
NM_001039213.4(CEACAM16):c.1122dup (p.Ala375fs)	rs1599814534
NM_001039213.4(CEACAM16):c.703dup (p.Arg235fs)

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