ClinVar Miner

List of variants in gene RUNX1 reported as uncertain significance by NIHR Bioresource Rare Diseases, University of Cambridge

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001754.5(RUNX1):c.484A>G (p.Arg162Gly)	rs1057519751
NM_001754.5(RUNX1):c.595G>A (p.Gly199Arg)	rs1601470582

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