ClinVar Miner

Submissions for variant NM_000370.3(TTPA):c.553-6C>T

gnomAD frequency: 0.00003  dbSNP: rs761911043
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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) RCV000732578 SCV000860549 uncertain significance not provided 2018-04-11 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000732578 SCV002382713 likely benign not provided 2024-03-09 criteria provided, single submitter clinical testing

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