ClinVar Miner

Submissions for variant NM_000043.6(FAS):c.30+19G>A

dbSNP: rs202165529
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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 RCV002124863 SCV002403678 benign Autoimmune lymphoproliferative syndrome type 1 2024-01-29 criteria provided, single submitter clinical testing

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