List of variants in gene TBX22 reported as likely benign for cleft palate with or without ankyloglossia, X-linked

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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001109878.2(TBX22):c.949+12T>G	rs151121450	0.01780
NM_001109878.2(TBX22):c.798+11T>C	rs199643713	0.00545
NM_001109878.2(TBX22):c.176-13C>A	rs55760411	0.00447
NM_001109878.2(TBX22):c.-23A>G	rs147593294	0.00280
NM_001109878.2(TBX22):c.356+6G>C	rs373965779	0.00171
NM_001109878.2(TBX22):c.1090C>T (p.Leu364=)	rs147281246	0.00075
NM_001109878.2(TBX22):c.799-13A>G	rs188139172	0.00038
NM_001109878.2(TBX22):c.240C>T (p.Tyr80=)	rs145373371	0.00021
NM_001109878.2(TBX22):c.1169C>A (p.Ala390Asp)	rs141303126	0.00011
NM_001109878.2(TBX22):c.-2-7C>A	rs185298778

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