ClinVar Miner

List of variants in gene RAD51C reported as likely pathogenic by Leiden Open Variation Database

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_058216.3(RAD51C):c.428A>G (p.Gln143Arg) rs587780255 0.00006
NM_058216.3(RAD51C):c.706-2A>G rs587780259 0.00002
NC_000017.11:g.(58724101_58732483)_(58732545_58734117)del

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