List of variants in gene IQCB1 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001023570.4(IQCB1):c.1441G>A (p.Glu481Lys)	rs140630401	0.00145
NM_001023570.4(IQCB1):c.1278+1G>A	rs1553711564
NM_001023570.4(IQCB1):c.1518_1519del (p.His506fs)	rs398123538
NM_001023570.4(IQCB1):c.214C>T (p.Arg72Ter)	rs201405662
NM_001023570.4(IQCB1):c.260T>G (p.Leu87Ter)	rs1553722736

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