List of variants in gene ITGA7 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_002206.3(ITGA7):c.3384C>T (p.Pro1128=)	rs148170949	0.00509
NM_002206.3(ITGA7):c.2644G>A (p.Glu882Lys)	rs144983062	0.00347
NM_002206.3(ITGA7):c.3058-6C>T	rs201070308	0.00252
NM_002206.3(ITGA7):c.882G>A (p.Val294=)	rs148190047	0.00223
NM_002206.3(ITGA7):c.2737C>T (p.Arg913Trp)	rs140030984	0.00169
NM_002206.3(ITGA7):c.1659C>G (p.Pro553=)	rs144052152	0.00075
NM_002206.3(ITGA7):c.537G>A (p.Gly179=)	rs145463677	0.00061
NM_002206.3(ITGA7):c.3174C>T (p.Leu1058=)	rs377148751	0.00006
NM_002206.3(ITGA7):c.63C>G (p.Ser21=)	rs368615107	0.00006
NM_002206.3(ITGA7):c.69C>T (p.Leu23=)	rs146932796	0.00006
NM_002206.3(ITGA7):c.2779C>T (p.Arg927Trp)	rs760407686	0.00001
NM_002206.3(ITGA7):c.1410-3del	rs773251917
NM_002206.3(ITGA7):c.671-295G>A
NM_002206.3(ITGA7):c.671-5C>A	rs180841797
NM_002206.3(ITGA7):c.762C>T (p.Ala254=)	rs376003902

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