ClinVar Miner

Submissions for variant NM_001101426.4(CRPPA):c.1251+50A>G

gnomAD frequency: 0.02578  dbSNP: rs78374272
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Preventiongenetics, part of Exact Sciences RCV000243778 SCV000306590 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001722297 SCV001948655 benign not provided 2018-07-07 criteria provided, single submitter clinical testing

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