List of variants in gene RUNX2 reported as 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: 27

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HGVS	dbSNP	gnomAD frequency
NM_001024630.4(RUNX2):c.423+268C>T	rs11498196	0.31316
NM_001024630.4(RUNX2):c.1021+46G>A	rs11498194	0.10376
NM_001024630.4(RUNX2):c.423+39G>C	rs3749864	0.08101
NM_001024630.4(RUNX2):c.59-1041T>C	rs7771980	0.07792
NM_001024630.4(RUNX2):c.423+255G>C	rs11498195	0.07586
NM_001024630.4(RUNX2):c.860-226T>G	rs73737447	0.07138
NM_001024630.4(RUNX2):c.686-264C>T	rs55930938	0.05021
NM_001024630.4(RUNX2):c.581-94A>T	rs77780637	0.04959
NM_001024630.4(RUNX2):c.59-672T>A	rs74865052	0.02884
NM_001024630.4(RUNX2):c.1022-299G>C	rs115553707	0.01649
NM_001024630.4(RUNX2):c.1531G>A (p.Gly511Ser)	rs11498198	0.00864
NM_001024630.4(RUNX2):c.1087+17T>C	rs148013252	0.00680
NM_001024630.4(RUNX2):c.663A>G (p.Val221=)	rs115763613	0.00499
NM_001024630.4(RUNX2):c.1166A>G (p.Asn389Ser)	rs115347084	0.00151
NM_001024630.4(RUNX2):c.*2845A>C	rs558458433	0.00073
NM_001024630.4(RUNX2):c.549C>T (p.Asn183=)	rs115974315	0.00067
NM_001024630.4(RUNX2):c.580+12A>G	rs189439261	0.00063
NM_001024630.4(RUNX2):c.*2619A>G	rs554964716	0.00059
NM_001024630.4(RUNX2):c.1021+13C>A	rs146099104	0.00050
NM_001024630.4(RUNX2):c.859+10A>T	rs200115506	0.00039
NM_001024630.4(RUNX2):c.336A>G (p.Glu112=)	rs368995035	0.00002
NM_001024630.4(RUNX2):c.933G>A (p.Thr311=)	rs146314825	0.00001
NM_001024630.4(RUNX2):c.348C>G (p.Thr116=)
NM_001024630.4(RUNX2):c.423+146_423+147dup	rs34916647
NM_001024630.4(RUNX2):c.423+17C>T	rs532943356
NM_001024630.4(RUNX2):c.423+22dup
NM_001024630.4(RUNX2):c.685+11C>T

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