ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.686+30C>T

gnomAD frequency: 0.01287  dbSNP: rs1800363
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001195048 SCV001950954 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001195048 SCV005272092 benign not provided criteria provided, single submitter not provided
Leiden Open Variation Database RCV001195048 SCV001365319 uncertain significance not provided 2020-02-28 no assertion criteria provided curation Curator: Arleen D. Auerbach. Submitter to LOVD: Arleen D. Auerbach.

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