ClinVar Miner

Submissions for variant NM_058195.4(CDKN2A):c.102G>A (p.Trp34Ter)

dbSNP: rs1820531050
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV001090490 SCV001246068 pathogenic not provided 2019-04-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001378150 SCV001575651 likely pathogenic Familial melanoma 2021-08-02 criteria provided, single submitter clinical testing

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