ClinVar Miner

Submissions for variant NM_001018115.3(FANCD2):c.3203T>C (p.Ile1068Thr)

dbSNP: rs2125060186
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001788948 SCV002030144 uncertain significance Fanconi anemia complementation group D2 2021-07-24 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

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