ClinVar Miner

Submissions for variant NM_004629.2(FANCG):c.1144-1G>C

dbSNP: rs755363896
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Leiden Open Variation Database RCV001194959 SCV001364830 pathogenic Fanconi anemia complementation group G 2011-02-07 no assertion criteria provided curation Curator: Arleen D. Auerbach. Submitter to LOVD: Arleen D. Auerbach.

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