List of variants in gene RUNX1 reported as likely benign by Illumina Laboratory Services, Illumina

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001754.5(RUNX1):c.*2193del	rs201977305	0.00589
NM_001754.5(RUNX1):c.1683_1684del	rs55761346	0.00208
NM_001754.5(RUNX1):c.303G>T (p.Val101=)	rs142472642	0.00200
NM_001754.5(RUNX1):c.*3977G>A	rs189557277	0.00011
NM_001754.5(RUNX1):c.*582del	rs201200981	0.00008
NM_001754.5(RUNX1):c.*3527T>G	rs548011352	0.00003
NM_001754.5(RUNX1):c.444C>T (p.Thr148=)	rs773689002	0.00002
NM_001754.5(RUNX1):c.*2201dup	rs201214658
NM_001754.5(RUNX1):c.*2467dup	rs200050352
NM_001754.5(RUNX1):c.*263C>G	rs527589424
NM_001754.5(RUNX1):c.*667del	rs200576340
NM_001754.5(RUNX1):c.*700dup	rs11424731
NM_001754.5(RUNX1):c.*730dup	rs11424730

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