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Rachel A. Veazey, MS, CGC is a general practitioner in Chapel Hill, NC specializing in obstetrics & gynecology, genetics and general practice. Rachel A. Veazey, MS, CGC is affiliated with UNC Health, UNC Hospitals and UNC Health Rex.
UNC Health Rex
She is certified by the Genetic Counseling, Board Certified.
Board Certification: Genetic Counseling, Board Certified (2022)
Rachel A. Veazey, MS, CGC appears to accept the following insurance providers: WellCare, AmeriHealth Caritas, Aetna, Humana, Cigna, BlueCross BlueShield of North Carolina (BCBSNC), MedCost, UnitedHealthcare, Carolina Complete Health, Liberty Advantage, Contigo Health, Veterans Affairs, Medicare Advantage, United Healthcare, Medicaid, OptumHealth Behavioral Solutions (United Behavioral Health), CHAMPVA, Centene, Group Health Plan (GHP), HealthTeam Advantage, MedCost PPO, FirstCarolinaCare Insurance Company Group Health Plans, North Carolina State Health Plan, BCBSNC Blue Home with UNC Health Alliance (Blue Home with Novant Health is out of network), FirstCarolinaCare FirstMedicare Direct, Contigo Health Plan (WakeMed employees only) (out-of-network beginning January 1, 2026), Aetna Premier Care Network Plus (APCN+) (Tier 2), BCBSNC Group Health Plans (except for Blue High Performance Network (BlueHPN)), Aetna Whole Health (Tier 2), Atlantic Packaging Corporation, Meritain Health, an Aetna Company, Longevity Health Plan I-SNP and Veterans Affairs Community Care Network.
According to our sources, Rachel A. Veazey, MS, CGC accepts the following insurance providers:
Rachel A. Veazey, MS, CGC has an exceptional overall rating with an average of 4.7 out of 5 stars based on 11 ratings. We collect ratings and reviews of Rachel A. Veazey, MS, CGC from all over the web to help you find the right in Chapel Hill, NC.
I am a prenatal and reproductive genetic counselor with over five years of experience. I work closely with families during and prior to pregnancy to guide and support them in learning about how inherited diseases and conditions might affect them and their families, in making decisions about testing, and in interpreting genetic test results based on their personal and family history.
