Variants in gene ITGA7 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_002206.3(ITGA7):c.2644G>A (p.Glu882Lys)	rs144983062	0.00347
NM_002206.3(ITGA7):c.2569G>A (p.Gly857Ser)	rs149081471	0.00270
NM_002206.3(ITGA7):c.1606C>T (p.Leu536Phe)	rs149028067	0.00083
NM_002206.3(ITGA7):c.2651A>T (p.Glu884Val)	rs149963176	0.00081
NM_002206.3(ITGA7):c.1722C>A (p.Ala574=)	rs142311782	0.00066
NM_002206.3(ITGA7):c.340A>G (p.Met114Val)	rs146565340	0.00063
NM_002206.3(ITGA7):c.537G>A (p.Gly179=)	rs145463677	0.00061
NM_002206.3(ITGA7):c.1317C>T (p.Phe439=)	rs200714716	0.00019
NM_002206.3(ITGA7):c.3263G>A (p.Arg1088Gln)	rs754655315	0.00005
NM_002206.3(ITGA7):c.2779C>T (p.Arg927Trp)	rs760407686	0.00001

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