List of variants in gene combination LOC130066607, RUNX1 reported as benign 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001754.5(RUNX1):c.-59-76A>G	rs56045941
NM_001754.5(RUNX1):c.-60+38dup	rs79420744

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