List of variants in gene combination ITGA2B, LOC130060983 reported as likely pathogenic for hematologic disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000419.5(ITGA2B):c.408G>C (p.Val136=)	rs1400938437	0.00001
NM_000419.5(ITGA2B):c.409-1G>A	rs1393747638	0.00001
NM_000419.5(ITGA2B):c.414C>A (p.Cys138Ter)	rs2048642260

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