List of variants in gene TBXAS1 reported as uncertain significance for hematologic disorder

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001061.7(TBXAS1):c.1520A>T (p.Glu507Val)	rs200663004	0.00044
NM_001061.7(TBXAS1):c.251G>T (p.Arg84Leu)	rs193110720	0.00004

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