ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.3480G>A (p.Val1160=)

dbSNP: rs1001303564
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001398987 SCV001600771 likely benign Ataxia-telangiectasia syndrome 2022-11-01 criteria provided, single submitter clinical testing

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