ClinVar Miner

Submissions for variant NM_004996.4(ABCC1):c.1988+890G>T

gnomAD frequency: 0.10946  dbSNP: rs4148353
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Research Lab, National Institute of Public Health RCV000123403 SCV000143790 association Familial cancer of breast 2014-02-01 no assertion criteria provided research

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