ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.23587T>C (p.Ser7863Pro) (rs1553906488)

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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic	RCV000660626	SCV000782746	uncertain significance	Limb-girdle muscular dystrophy, type 2J	2017-09-21	criteria provided, single submitter	clinical testing

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