ClinVar Miner

List of variants in gene BRIP1 reported as likely benign for Familial ovarian cancer

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.1935+11G>A	rs79121306	0.00051
NM_032043.3(BRIP1):c.1455T>C (p.Ala485=)	rs773489367	0.00001

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