ClinVar Miner

Submissions for variant NC_000001.11:g.172658358C>T

gnomAD frequency: 0.49239  dbSNP: rs763110
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
Labcorp Genetics (formerly Invitae), Labcorp RCV001511738 SCV001719034 benign Autoimmune lymphoproliferative syndrome type 1 2024-01-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004715433 SCV005288507 benign not provided criteria provided, single submitter not provided

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