List of variants in gene TBX2 reported as benign for Vertebral anomalies and variable endocrine and T-cell dysfunction

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_005994.4(TBX2):c.1687-22C>T	rs2240736	0.66949
NM_005994.4(TBX2):c.1827C>T (p.Ser609=)	rs1057987	0.59551
NM_005994.4(TBX2):c.1051+43G>A	rs9891115	0.55949
NM_005994.4(TBX2):c.1051+39C>G	rs35619711	0.55927
NM_005994.4(TBX2):c.1051+36del	rs66504335	0.53283

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