List of variants in gene TBX22 reported as uncertain significance for bone disorder

Minimum submission review status:		Collection method:
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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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001109878.2(TBX22):c.1488C>T (p.Asp496=)	rs35602350	0.00128
NM_001109878.2(TBX22):c.-28G>A	rs746947861	0.00092
NM_001109878.2(TBX22):c.*97C>A	rs757571902	0.00053
NM_001109878.2(TBX22):c.*533A>T	rs770782241	0.00023
NM_001109878.2(TBX22):c.1544C>A (p.Ala515Glu)	rs201336957	0.00019
NM_001109878.2(TBX22):c.302T>A (p.Leu101Gln)	rs137989876	0.00016
NM_001109878.2(TBX22):c.864-11C>T	rs771601265	0.00008
NM_001109878.2(TBX22):c.452G>T (p.Arg151Leu)	rs368136178	0.00005
NM_001109878.2(TBX22):c.554C>T (p.Ser185Leu)	rs765734398	0.00002
NM_001109878.2(TBX22):c.*293T>C	rs1259520333	0.00001
NM_001109878.2(TBX22):c.1412C>T (p.Ser471Phe)	rs1057515990	0.00001
NM_001109878.2(TBX22):c.448A>C (p.Lys150Gln)	rs1156605251	0.00001
NM_001109878.2(TBX22):c.549C>G (p.Pro183=)	rs146024976	0.00001
NM_001109878.2(TBX22):c.*57A>T	rs1057515991
NM_001109878.2(TBX22):c.143G>A (p.Arg48Lys)	rs1923753821
NM_001109878.2(TBX22):c.224G>T (p.Gly75Val)	rs1923802331
NM_001109878.2(TBX22):c.592C>T (p.Arg198Cys)	rs776905471

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