List of variants in gene IVNS1ABP reported as pathogenic by OMIM

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
NC_000001.10:g.185276239_185287961del
NM_006469.5(IVNS1ABP):c.1072C>T (p.Arg358Ter)	rs756921311
NM_006469.5(IVNS1ABP):c.1899G>A (p.Trp633Ter)	rs1665467187

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