List of variants in gene RUNX1 reported as benign by Genetic Services Laboratory, University of Chicago

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001754.5(RUNX1):c.183G>A (p.Pro61=)	rs76558016	0.00454
NM_001754.5(RUNX1):c.144C>T (p.Ser48=)	rs147889692	0.00332
NM_001754.5(RUNX1):c.303G>T (p.Val101=)	rs142472642	0.00200
NM_001754.5(RUNX1):c.1269C>T (p.Arg423=)	rs544247912	0.00040
NM_001754.5(RUNX1):c.1355T>G (p.Val452Gly)	rs751710767	0.00004

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