ClinVar Miner

Submissions for variant NM_005850.4(SF3B4):c.-116C>T

gnomAD frequency: 0.01701  dbSNP: rs60631776
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
GeneDx RCV001612445 SCV001841325 benign not provided 2020-11-01 criteria provided, single submitter clinical testing

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