ClinVar Miner

Submissions for variant NM_015272.5(RPGRIP1L):c.882+12A>G

gnomAD frequency: 0.00001  dbSNP: rs1264347960
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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 RCV002103298 SCV002389437 likely benign Familial aplasia of the vermis; Meckel-Gruber syndrome 2022-12-16 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494201 SCV002803304 likely benign Joubert syndrome 7; Meckel syndrome, type 5; COACH syndrome 3 2021-10-08 criteria provided, single submitter clinical testing

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