ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.96868G>A (p.Glu32290Lys)

dbSNP: rs1060500512
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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 RCV000469309 SCV000542816 uncertain significance Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2016-09-15 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV003139630 SCV003820324 uncertain significance not provided 2019-04-29 criteria provided, single submitter clinical testing

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