ClinVar Miner

List of variants in gene combination BRCA1, LOC111589215 reported as uncertain significance for breast-ovarian cancer, familial, susceptibility to, 1

Included ClinVar conditions (7):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
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HGVS dbSNP gnomAD frequency
NM_007294.4(BRCA1):c.-86C>T rs143160357 0.00077
NM_007294.4(BRCA1):c.-20+11C>T rs273898672 0.00042
NM_007294.3(BRCA1):c.-125C>T rs148196794 0.00017
NM_007294.4(BRCA1):c.-20+103G>C rs1057517546 0.00001
NM_007294.4(BRCA1):c.-75C>G rs529629382 0.00001
NM_007294.4(BRCA1):c.-20+101_-20+102delinsGC rs1057517555
NM_007294.4(BRCA1):c.-20+102dup rs759063490
NM_007294.4(BRCA1):c.-20+103G>A rs1057517546
NM_007294.4(BRCA1):c.-20+13C>T rs770368390
NM_007294.4(BRCA1):c.-20+59G>T rs1057517547
NM_007294.4(BRCA1):c.-22A>G rs886052976
NM_007294.4(BRCA1):c.-42T>G rs544342552

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