ClinVar Miner

List of variants reported as pathogenic for Fanconi anemia complementation group G by OMIM

Included ClinVar conditions (1):
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Total variants: 8
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HGVS dbSNP
FANCG, IVS13, G-C, -1
NM_004629.1(FANCG):c.1066C>T (p.Gln356Ter) rs121434426
NM_004629.1(FANCG):c.1480+1G>C rs149616199
NM_004629.1(FANCG):c.1795_1804del (p.Trp599Profs) rs397507560
NM_004629.1(FANCG):c.307+1G>C rs200479612
NM_004629.1(FANCG):c.313G>T (p.Glu105Ter) rs121434425
NM_004629.1(FANCG):c.637_643del (p.Tyr213fs) rs587776640
NM_004629.1(FANCG):c.925-2A>G rs397507561

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