ClinVar Miner

Submissions for variant NM_001330311.2(DVL1):c.366A>G (p.Pro122=)

gnomAD frequency: 0.99656  dbSNP: rs307362
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001514850 SCV001722793 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV001514850 SCV001753373 benign not provided 2018-09-17 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001544075 SCV001763048 benign Autosomal dominant Robinow syndrome 2 2021-07-14 criteria provided, single submitter clinical testing

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