ClinVar Miner

Submissions for variant NM_022772.4(EPS8L2):c.165+10C>T

gnomAD frequency: 0.00018  dbSNP: rs376112350
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002178382 SCV002479172 likely benign not provided 2023-12-31 criteria provided, single submitter clinical testing

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