ClinVar Miner

List of variants in gene combination FANCG, VCP reported as uncertain significance for anemia (disease)

Included ClinVar conditions (281):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
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NM_004629.1(FANCG):c.1538G>A (p.Arg513Gln) rs17885240
NM_004629.1(FANCG):c.1638T>C (p.Gly546=) rs45537335

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