List of variants in gene TBX19 reported as uncertain significance by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_005149.3(TBX19):c.1310C>T (p.Ala437Val)	rs147003438	0.00005
NM_005149.3(TBX19):c.916+2T>G	rs763382655	0.00001
NM_005149.3(TBX19):c.210G>T (p.Met70Ile)	rs1558190316
NM_005149.3(TBX19):c.477G>C (p.Leu159Phe)	rs1558190989
NM_005149.3(TBX19):c.562G>A (p.Glu188Lys)	rs1159356681

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