List of variants in gene CLDN9 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_020982.4(CLDN9):c.346C>T (p.Arg116Cys)
NM_020982.4(CLDN9):c.370_372dup (p.Ile124dup)	rs773682747
NM_020982.4(CLDN9):c.500dup (p.Trp168fs)	rs1567404609

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