ClinVar Miner

Submissions for variant NM_001330311.2(DVL1):c.-45C>T

gnomAD frequency: 0.80772  dbSNP: rs150789461
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001544210 SCV001763203 benign Autosomal dominant Robinow syndrome 2 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001685490 SCV001901834 benign not provided 2018-10-16 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001685490 SCV005286075 benign not provided criteria provided, single submitter not provided

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