ClinVar Miner

List of variants in gene RUNX2 studied for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001024630.4(RUNX2):c.423+39G>C	rs3749864	0.08101
NM_001024630.4(RUNX2):c.423+3A>G	rs1231715575	0.00001
NM_001024630.4(RUNX2):c.886C>T (p.Pro296Ser)	rs1554397657

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