ClinVar Miner

Submissions for variant NM_003560.4(PLA2G6):c.1241G>T (p.Cys414Phe)

dbSNP: rs1569258633
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001579703 SCV001808189 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001579703 SCV001972600 likely benign not provided no assertion criteria provided clinical testing

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