ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.10878T>C (p.Val3626=)

dbSNP: rs1334951450
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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 RCV001454625 SCV001658358 likely benign Cohen syndrome 2024-01-01 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003955991 SCV004783933 likely benign VPS13B-related disorder 2022-12-27 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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