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rs137852986(C;T)

From SNPedia
Increased cancer risk; ovarian cancer & related
Is agenotype
ofrs137852986
GeneBRIP1
Chromosome17
Position61,716,051
mentionedby
Magnitude6
ReputeBad
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 6 Increased cancer risk; ovarian cancer & related

This is a genotype with recommended actions if clinically confirmed. In brief:

  • Three genes (BRIP1, RAD51C and RAD51D) may contain mutations increasing risk of ovarian cancer; this genotype includes one such mutation.
  • The lifetime risk of ovarian cancer in carriers of such mutations appears to be high enough to consider risk-reducing salpingo-oophorectomy (RRSO) surgery.
  • It's unclear when the best time to consider such surgery is, but perhaps carriers of RAD51C, RAD51D, or BRIP1 pathogenic variants should consider RRSO around age 45–50 years or earlier based on a specific family history of an earlier onset ovarian cancer.
  • While the relative risk of ovarian cancer is around 6x or 10x higher in RAD51C/D or BRIP1 mutation carriers relative to non-carriers, the cumulative lifetime risk appears to remain under 10% up to age 80 in the absence of family history.
  • The decision to carry out RRSO should not be made lightly, given the impact of premature menopause and related issues such as surgical complications, worsening of vasomotor symptoms, and decreased sexual functioning.


The full ClinGen Actionability report about BRIP1, RAD51C, and RAD51D with respect to ovarian cancer can be found here.

Genetic counseling may be available to you through your health-care network. Additional information is available via our Find A Genetic Counselor webpage, located here.