ClinVar Miner

Submissions for variant NM_015352.2(POFUT1):c.736-12C>T

gnomAD frequency: 0.00011  dbSNP: rs370903391
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002199670 SCV002356328 benign Dowling-Degos disease 2 2024-01-24 criteria provided, single submitter clinical testing

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