List of variants in gene IQCB1 reported as uncertain significance for Renal dysplasia and retinal aplasia

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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_001023570.4(IQCB1):c.-147del	rs886057829	0.00161
NM_001023570.3(IQCB1):c.-215C>T	rs541891117	0.00029
NM_001023570.4(IQCB1):c.1344A>G (p.Gln448=)	rs886057824	0.00001
NM_001023570.4(IQCB1):c.488-13dup	rs753164790

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