ClinVar Miner

Submissions for variant NM_006180.6(NTRK2):c.1396+10del

dbSNP: rs781678424
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002129839 SCV002404243 benign not provided 2024-11-11 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494276 SCV002800013 likely benign Obesity, hyperphagia, and developmental delay; Developmental and epileptic encephalopathy, 58 2021-09-28 criteria provided, single submitter clinical testing

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