ClinVar Miner

Submissions for variant NC_000011.10:g.5225460A>C

gnomAD frequency: 0.00056  dbSNP: rs560643693
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000876346 SCV001018909 likely benign not provided 2024-01-24 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV001001384 SCV001134208 benign not specified 2019-11-12 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000876346 SCV001158586 benign not provided 2020-04-02 criteria provided, single submitter clinical testing

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