ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.30835G>A (p.Glu10279Lys)

gnomAD frequency: 0.00001  dbSNP: rs1387185323
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000729513 SCV000857183 uncertain significance not provided 2017-09-30 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV005240512 SCV005885380 uncertain significance not specified 2025-02-24 criteria provided, single submitter clinical testing

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