ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.33975G>A (p.Val11325=)

dbSNP: rs1560303919
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000730354 SCV000858083 uncertain significance not provided 2017-11-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002060993 SCV002376535 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2021-07-16 criteria provided, single submitter clinical testing

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