ClinVar Miner

Submissions for variant NM_004629.2(FANCG):c.1366del (p.His456fs)

dbSNP: rs587778345
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV004567045 SCV005057683 likely pathogenic Fanconi anemia complementation group G 2024-02-08 criteria provided, single submitter clinical testing
ITMI RCV000121033 SCV000085201 not provided not specified 2013-09-19 no assertion provided reference population

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