ClinVar Miner

Submissions for variant NM_000489.6(ATRX):c.7200+9del

dbSNP: rs781816667
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000729120 SCV000856760 uncertain significance not provided 2017-09-21 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001476348 SCV001680556 likely benign Alpha thalassemia-X-linked intellectual disability syndrome 2024-09-27 criteria provided, single submitter clinical testing

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