ClinVar Miner

Submissions for variant NM_001083116.3(PRF1):c.539+22G>C

dbSNP: rs12263464
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000247668 SCV000306476 likely benign not specified criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316376 SCV004017104 likely benign Lymphoma, non-Hodgkin, familial 2023-07-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004705086 SCV005228148 likely benign not provided criteria provided, single submitter not provided

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