ClinVar Miner

List of variants in gene RAD51D studied for breast-ovarian cancer, familial, susceptibility to, 4

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
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HGVS dbSNP gnomAD frequency
NC_000017.10:g.(?_33427972)_(33428065_?)del
NC_000017.10:g.(?_33427972)_(33428404_?)del
NC_000017.10:g.(?_33427972)_(33430573_?)del
NC_000017.10:g.(?_33427972)_(33434476_?)del
NC_000017.10:g.(?_33427972)_(33446632_?)dup
NC_000017.10:g.(?_33430263)_(33430573_?)del
NC_000017.10:g.(?_33430263)_(33446632_?)dup
NC_000017.10:g.(?_33430267)_(33446638_?)del
NC_000017.10:g.(?_33443985)_(33446632_?)del
NC_000017.10:g.(?_33445500)_(33446632_?)dup
NC_000017.10:g.(?_33446541)_(33446632_?)del
NC_000017.11:g.(?_35100943)_(35119623_?)del
NC_000017.11:g.(?_35100953)_(35119613_?)del
NC_000017.11:g.(?_35103244)_(35119613_?)del
NC_000017.11:g.(?_35106376)_(35107457_?)del
NC_000017.11:g.(?_35116966)_(35118629_?)del
NM_001142571.1:c.637_1047del
NM_001142571.1:c.963_1047del
NM_002878.3:c.(903+1_904-1)_(*1161_?)del
NM_002878.4:c.(263_263+1459)_(263+1647_264)del
NM_002878.4:c.1_263del
NM_002878.4:c.1_987del
NM_002878.4:c.740_987del
NM_002878.4:c.82_577-1del

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