ClinVar Miner

Submissions for variant NM_020408.6(LYRM4):c.-11_-10dup

dbSNP: rs561083109
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001714252 SCV001944229 benign not provided 2018-06-06 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002503168 SCV002811222 likely benign Combined oxidative phosphorylation defect type 14; Hereditary spastic paraplegia 77 2021-07-26 criteria provided, single submitter clinical testing

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