List of variants in gene RUNX1 reported as likely benign for immune system cancer

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001754.5(RUNX1):c.952T>G (p.Ser318Ala)	rs545554349	0.00013
NM_001754.5(RUNX1):c.1005G>T (p.Gln335His)	rs80314254	0.00011
NM_001754.5(RUNX1):c.1252A>G (p.Met418Val)	rs578042376	0.00010
NM_001754.5(RUNX1):c.492C>T (p.Val164=)	rs200907577	0.00008
NM_001754.5(RUNX1):c.1338C>T (p.Leu446=)	rs769628054	0.00004
NM_001754.5(RUNX1):c.1272G>C (p.Ser424=)	rs1459260782
NM_001754.5(RUNX1):c.154A>G (p.Met52Val)

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