ClinVar Miner

Submissions for variant NM_001330227.2(NUCB2):c.-254A>G

gnomAD frequency: 0.13527  dbSNP: rs4757506
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Research Center, Shahid Beheshti University of Medical Sciences RCV000114968 SCV000148859 untested not provided no assertion provided not provided Converted during submission to not provided.

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