List of variants in gene RUNX2 reported as benign by PreventionGenetics, part of Exact Sciences

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001024630.4(RUNX2):c.423+39G>C	rs3749864	0.08101
NM_001024630.4(RUNX2):c.663A>G (p.Val221=)	rs115763613	0.00499
NM_001024630.4(RUNX2):c.685+26426G>A
NM_001024630.4(RUNX2):c.685+26477C>T

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