ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.588del (p.Gly197fs)

dbSNP: rs1057516683
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000411087 SCV000486062 likely pathogenic Ataxia-telangiectasia syndrome 2016-03-22 criteria provided, single submitter clinical testing
Laboratory for Genotyping Development, RIKEN RCV003168590 SCV002758387 pathogenic Gastric cancer 2021-07-01 no assertion criteria provided research

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