ClinVar Miner

Submissions for variant NM_001018115.3(FANCD2):c.206-1G>T

dbSNP: rs2124974541
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Dept. of Cytogenetics, ICMR- National Institute of Immunohaematology RCV001615373 SCV001832592 likely pathogenic Fanconi anemia criteria provided, single submitter clinical testing
Baylor Genetics RCV003470873 SCV004196751 likely pathogenic Fanconi anemia complementation group D2 2023-05-23 criteria provided, single submitter clinical testing

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