Variants in gene ITGB4 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 3

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HGVS	dbSNP	gnomAD frequency
NM_000213.5(ITGB4):c.2701C>T (p.Leu901Phe)	rs145644205	0.00272
NM_000213.5(ITGB4):c.1940C>T (p.Thr647Met)
NM_000213.5(ITGB4):c.2422G>A (p.Ala808Thr)	rs147480547

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