List of variants in gene RUNX1 reported as likely benign for not provided

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_001754.5(RUNX1):c.613+158C>T	rs56138997	0.02118
NM_001754.5(RUNX1):c.508+169G>A	rs113118471	0.01414
NM_001754.5(RUNX1):c.167T>C (p.Leu56Ser)	rs111527738	0.01206
NM_001754.5(RUNX1):c.508+275T>G	rs75181041	0.01122
NM_001754.5(RUNX1):c.927C>T (p.Gly309=)	rs59802347	0.01119
NM_001754.5(RUNX1):c.509-197T>C	rs55961764	0.00960
NM_001754.5(RUNX1):c.*121G>C	rs549844608	0.00871
NM_001754.5(RUNX1):c.*44C>G	rs535532916	0.00869
NM_001754.5(RUNX1):c.613+108G>A	rs111433804	0.00757
NM_001754.5(RUNX1):c.58+23A>G	rs117776183	0.00482
NM_001754.5(RUNX1):c.508+182A>G	rs76637156	0.00473
NM_001754.5(RUNX1):c.144C>T (p.Ser48=)	rs147889692	0.00344
NM_001754.5(RUNX1):c.613+8C>T	rs186585782	0.00300
NM_001754.5(RUNX1):c.303G>T (p.Val101=)	rs142472642	0.00200
NM_001754.5(RUNX1):c.654C>T (p.Ser218=)	rs145230602	0.00063
NM_001754.5(RUNX1):c.1269C>T (p.Arg423=)	rs544247912	0.00040
NM_001754.5(RUNX1):c.648C>T (p.Pro216=)	rs199759556	0.00021
NM_001754.5(RUNX1):c.508+18A>G	rs377681816	0.00012
NM_001754.5(RUNX1):c.668A>G (p.Glu223Gly)	rs780999703	0.00009
NM_001754.5(RUNX1):c.1190A>G (p.Gln397Arg)	rs762292084	0.00008
NM_001754.5(RUNX1):c.552G>T (p.Pro184=)	rs752586117	0.00006
NM_001754.5(RUNX1):c.900G>A (p.Thr300=)	rs533383085	0.00001
NC_000021.9:g.35049405_35049406del	rs57713477
NM_001754.5(RUNX1):c.-19G>A	rs1568815605
NM_001754.5(RUNX1):c.1437C>T (p.Pro479=)	rs1601331827
NM_001754.5(RUNX1):c.165G>A (p.Ala55=)	rs766206710
NM_001754.5(RUNX1):c.98-1411_98-1410del	rs377766157
NM_001754.5(RUNX1):c.98-1418dup	rs377766157
NM_001754.5(RUNX1):c.98-148_98-147dup

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