ClinVar Miner

Submissions for variant NM_022662.4(ANAPC1):c.685+25A>G

dbSNP: rs6742515
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001553991 SCV001775124 benign Rothmund-Thomson syndrome type 1 2021-07-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004709108 SCV005239497 benign not provided criteria provided, single submitter not provided

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