List of variants in gene ABL1 reported as pathogenic by GeneDx

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_005157.6(ABL1):c.1009G>A (p.Ala337Thr)	rs1060499548
NM_005157.6(ABL1):c.1388G>A (p.Gly463Asp)	rs2133017541
NM_005157.6(ABL1):c.1525G>A (p.Glu509Lys)	rs1831433011
NM_005157.6(ABL1):c.350C>T (p.Thr117Met)	rs1830948350
NM_005157.6(ABL1):c.677A>G (p.Tyr226Cys)	rs1060499547
NM_005157.6(ABL1):c.730A>G (p.Met244Val)	rs121913456

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