ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.32371G>C (p.Val10791Leu)

dbSNP: rs765062133
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Phosphorus, Inc. RCV000578105 SCV000679963 uncertain significance Dilated cardiomyopathy 1G 2017-08-01 criteria provided, single submitter clinical testing
Phosphorus, Inc. RCV000577989 SCV000679964 uncertain significance Autosomal recessive limb-girdle muscular dystrophy type 2J 2017-08-01 criteria provided, single submitter clinical testing
Phosphorus, Inc. RCV000578051 SCV000679965 uncertain significance Tibial muscular dystrophy 2017-08-01 criteria provided, single submitter clinical testing

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