List of variants reported as likely pathogenic for breast-ovarian cancer, familial, susceptibility to, 1 by Department of Medical Genetics, Oslo University Hospital

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NC_000017.10:g.(41228632_41234420)_(41234593_41242960)dup
NM_007294.4(BRCA1):c.115T>G (p.Cys39Gly)	rs80357164
NM_007294.4(BRCA1):c.140G>T (p.Cys47Phe)	rs80357150
NM_007294.4(BRCA1):c.213-5T>A	rs886038196
NM_007294.4(BRCA1):c.5074+2T>C	rs80358089
NM_007294.4(BRCA1):c.5153G>C (p.Trp1718Ser)	rs41293461
NM_007294.4(BRCA1):c.5212G>A (p.Gly1738Arg)	rs80356937
NM_007294.4(BRCA1):c.5213G>A (p.Gly1738Glu)	rs80357450
NM_007294.4(BRCA1):c.5309G>T (p.Gly1770Val)	rs863224765
NM_007294.4(BRCA1):c.5513T>G (p.Val1838Gly)	rs80357107
NM_007294.4(BRCA1):c.65T>C (p.Leu22Ser)	rs80357438
Single allele

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