ClinVar Miner

Submissions for variant NM_000371.3(TTR):c.337-18G>C (rs36204272)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Integrated Genetics/Laboratory Corporation of America RCV000030574 SCV000053249 benign Cardiomyopathy 2011-08-18 criteria provided, single submitter curation Converted during submission to Benign.
PreventionGenetics,PreventionGenetics RCV000248110 SCV000303886 benign not specified 2016-04-04 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000248110 SCV000332774 benign not specified 2015-07-06 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001283523 SCV001157234 benign none provided 2020-09-01 criteria provided, single submitter clinical testing
Molecular Genetics Laboratory,London Health Sciences Centre RCV001173542 SCV001336632 benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing

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