List of variants in gene CIB2 reported as likely pathogenic for perceptual disorders

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_006383.4(CIB2):c.556C>T (p.Arg186Trp)	rs370359511	0.00024
NM_006383.4(CIB2):c.196C>T (p.Arg66Trp)	rs780168150	0.00003
NM_006383.4(CIB2):c.272T>C (p.Phe91Ser)	rs397515411	0.00003
NM_006383.4(CIB2):c.300_309del (p.Glu100fs)	rs765741202	0.00003
NM_006383.4(CIB2):c.297C>G (p.Cys99Trp)	rs370965183
NM_006383.4(CIB2):c.383_384insTA (p.Glu129fs)

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