ClinVar Miner

Submissions for variant NM_002529.3(NTRK1):c.570C>G (p.Ser190Arg) (rs138608619)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000291812 SCV000349042 uncertain significance Hereditary insensitivity to pain with anhidrosis 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000291812 SCV000752382 likely benign Hereditary insensitivity to pain with anhidrosis 2017-09-06 criteria provided, single submitter clinical testing
Mendelics RCV000708810 SCV000837796 uncertain significance Familial medullary thyroid carcinoma 2018-07-02 criteria provided, single submitter clinical testing

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