ClinVar Miner

List of variants in gene combination BRK1, FANCD2, FANCD2OS, LOC107303338, LOC107303339, LOC107303340, VHL reported as pathogenic for Fanconi anemia

Included ClinVar conditions (38):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP
NC_000003.11:g.(?_10106407)_(10188326_?)del

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