ClinVar Miner

List of variants in gene combination FANCD2, FANCD2OS reported as benign for anemia (disease)

Included ClinVar conditions (258):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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HGVS dbSNP
NM_001018115.2(FANCD2):c.3849+13A>G rs9811771
NM_001018115.2(FANCD2):c.4098T>G (p.Leu1366=) rs2272125
NM_033084.4(FANCD2):c.*37G>A rs7626117
NM_033084.4(FANCD2):c.*431T>G rs3826
NM_033084.4(FANCD2):c.*538G>A rs9862958
NM_033084.4(FANCD2):c.*550C>T rs11716842
NM_033084.4(FANCD2):c.*62A>G rs7647987
NM_033084.4(FANCD2):c.3446C>T (p.Ala1149Val) rs147675860
NM_033084.4(FANCD2):c.4038+8G>A rs190990145

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