List of variants in gene combination ITGA2B, LOC130060983 reported as uncertain significance for blood coagulation disease

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000419.5(ITGA2B):c.408+16C>T	rs377288289	0.00014
NM_000419.5(ITGA2B):c.408G>C (p.Val136=)	rs1400938437	0.00001
NM_000419.5(ITGA2B):c.408+11C>A	rs768343439
NM_000419.5(ITGA2B):c.409-3C>G	rs2143489585
NM_000419.5(ITGA2B):c.413G>T (p.Cys138Phe)

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