ClinVar Miner

Submissions for variant NM_005157.6(ABL1):c.1766G>A (p.Arg589His)

gnomAD frequency: 0.00012  dbSNP: rs376925416
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002055323 SCV002421253 likely benign not provided 2025-01-20 criteria provided, single submitter clinical testing
ITMI RCV000119948 SCV000084078 not provided not specified 2013-09-19 no assertion provided reference population

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