ClinVar Miner

Submissions for variant NM_000043.6(FAS):c.444-5del

dbSNP: rs751798922
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000289101 SCV000365902 uncertain significance Autoimmune lymphoproliferative syndrome type 1 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000289101 SCV002406656 benign Autoimmune lymphoproliferative syndrome type 1 2023-11-28 criteria provided, single submitter clinical testing

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