List of variants in gene LOC109611593, RUNX2, SUPT3H studied for bone development disease

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001024630.4(RUNX2):c.-120T>C	rs535015975	0.00005
NM_001024630.4(RUNX2):c.-66-14G>T	rs768238770

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