List of variants in gene ITGB4 reported as likely pathogenic by GeneDx

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_000213.5(ITGB4):c.884_885del (p.Thr295fs)	rs1377620586	0.00001
NM_000213.5(ITGB4):c.599C>A (p.Pro200His)	rs148770294
NM_000213.5(ITGB4):c.950ACA[1] (p.Asn318del)	rs778801524

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