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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 12

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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.3112-3C>T	rs151033645	0.00138
NM_000213.5(ITGB4):c.1345G>A (p.Gly449Ser)	rs147963396	0.00135
NM_000213.5(ITGB4):c.2638G>A (p.Asp880Asn)	rs139092703	0.00086
NM_000213.5(ITGB4):c.3427A>G (p.Ile1143Val)	rs149481974	0.00056
NM_000213.5(ITGB4):c.1666C>T (p.Arg556Cys)	rs150166497	0.00038
NM_000213.5(ITGB4):c.2834G>A (p.Arg945Gln)	rs141953294	0.00006
NM_000213.5(ITGB4):c.3221G>A (p.Arg1074His)	rs147026529	0.00004
NM_000213.5(ITGB4):c.2422G>A (p.Ala808Thr)	rs147480547
NM_000213.5(ITGB4):c.2521G>A (p.Ala841Thr)
NM_000213.5(ITGB4):c.3265G>C (p.Gly1089Arg)
NM_000213.5(ITGB4):c.599C>T (p.Pro200Leu)	rs148770294

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