ClinVar Miner

List of variants reported as uncertain significance by Department of Pathology and Genetics, University of Gothenburg

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_000135.4(FANCA):c.2728C>T (p.Leu910Phe) rs1216426444
NM_000135.4(FANCA):c.4261-2A>C rs915983602

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