ClinVar Miner

Submissions for variant NM_032861.4(SERAC1):c.1404-175A>G

gnomAD frequency: 0.00583  dbSNP: rs114701992
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
GeneDx RCV001559948 SCV001782275 likely benign not provided 2018-07-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001559948 SCV005226228 likely benign not provided criteria provided, single submitter not provided

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