ClinVar Miner

Submissions for variant NM_007214.5(SEC63):c.1936-11_1936-9del

dbSNP: rs749125299
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000946965 SCV001093128 benign not provided 2017-05-08 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002489290 SCV002794627 likely benign Polycystic liver disease 2 2021-10-04 criteria provided, single submitter clinical testing

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