List of variants in gene ABL1 reported as likely benign for hematologic disorder

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_005157.6(ABL1):c.1899C>T (p.Ala633=)	rs2229068	0.00732
NM_005157.6(ABL1):c.249T>G (p.Thr83=)	rs111886835	0.00382
NM_005157.6(ABL1):c.822+16C>G	rs12551730	0.00309
NM_005157.6(ABL1):c.2117G>T (p.Gly706Val)	rs34634745	0.00014
NM_005157.6(ABL1):c.2035T>G (p.Ser679Ala)	rs201278085

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