ClinVar Miner

Submissions for variant NM_005654.6(NR2F1):c.*9C>T

dbSNP: rs202006298
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
GeneDx RCV000712441 SCV000526132 benign not provided 2020-04-10 criteria provided, single submitter clinical testing
Athena Diagnostics RCV000712441 SCV000842937 benign not provided 2018-06-07 criteria provided, single submitter clinical testing

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