ClinVar Miner

Submissions for variant NC_000010.11:g.88990206A>G

gnomAD frequency: 0.54268  dbSNP: rs1800682
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001515574 SCV001723672 benign Autoimmune lymphoproliferative syndrome type 1 2020-12-06 criteria provided, single submitter clinical testing

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