ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.39709+4C>T

dbSNP: rs1553768226
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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 RCV000643780 SCV000765467 uncertain significance Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2018-01-06 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004692014 SCV005188140 uncertain significance not provided criteria provided, single submitter not provided

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