ClinVar Miner

Submissions for variant NM_020442.6(VARS2):c.969C>T (p.Pro323=)

gnomAD frequency: 0.00214  dbSNP: rs148701242
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001787561 SCV002030991 likely benign not provided 2021-06-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001787561 SCV002452334 benign not provided 2024-01-22 criteria provided, single submitter clinical testing

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