ClinVar Miner

Submissions for variant NM_004996.4(ABCC1):c.1218+9C>T

gnomAD frequency: 0.00003  dbSNP: rs483352877
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
Invitae RCV000119782 SCV001068459 likely benign not provided 2018-06-22 criteria provided, single submitter clinical testing
Department of Molecular Biophysics, University of Lodz RCV000119782 SCV000154689 not provided not provided no assertion provided not provided

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