List of variants in gene ITGA7 reported as likely pathogenic for not provided

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_002206.3(ITGA7):c.1088del (p.Gly363fs)	rs587780362
NM_002206.3(ITGA7):c.1446_1453del (p.Ile483fs)	rs1474512248
NM_002206.3(ITGA7):c.253del (p.Ala85fs)
NM_002206.3(ITGA7):c.2761C>T (p.Gln921Ter)	rs767943997
NM_002206.3(ITGA7):c.463G>T (p.Glu155Ter)
NM_002206.3(ITGA7):c.94_95dup (p.Ala33fs)	rs2136102892

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