RHeference
  • Allele
    • List
    • Search
  • References
    • All
    • By Author
    • By Journal
  • Documentation
  • Statistics
  • Search
    • By name
    • By mutation
    • In exons
    • Complex
  • Contact

Article

Systematic RH genotyping and variant identification in French donors of African origin. Kappler-Gratias S, Auxerre C, Dubeaux I, Beolet M, Ripaux M, Le Pennec PY, Pham BN. Blood Transfus, 2014. [Citation]

Annotations by Allele

  • RHD deletion (RHD*01N.01): RH1 (adsorption-elution was not performed)
  • RHD deletion (RHD*01N.01): Prevalence
  • RHD*1136T (DAU0): RH1
  • RHD*1136T (DAU0): Prevalence
  • RHD*186T,410T,455C,1048C (DIVa): RH1
  • RHD*186T,410T,455C,1048C (DIVa): Prevalence
  • RHD*186T,410T,455C,602G,667G,819A (DIIIa): RH1
  • RHD*186T,410T,455C,602G,667G,819A (DIIIa): Prevalence
  • RHD*509C,667G,1132G (DOL2, RHD*12.02): Prevalence
  • RHD*509C,667G,1132G (DOL2, RHD*12.02): RH1
  • RHD*579A,1136T (DAU0.01): Prevalence
  • RHD*602G,667G,744T,957A,1025C (weak D type 4.2.2, DAR1.02): RH1
  • RHD*602G,667G,744T,957A,1025C (weak D type 4.2.2, DAR1.02): Prevalence
  • RHD*602G,667G,819A (weak D type 4.0, DAR3.01): RH1
  • RHD*602G,667G,819A (weak D type 4.0, DAR3.01): Prevalence
  • RHD*667G (DFV, RHD*08.01): Prevalence
  • RHD*667G (DFV, RHD*08.01): RH1
  • RHD*667G,697C (DV type 1, Kou): RH1
  • RHD*667G,697C (DV type 1, Kou): Prevalence
  • RHD*667G,697C,1136T (DAU5): RH1
  • RHD*667G,697C,1136T (DAU5): Prevalence
  • RHD*835A,1136T (DAU3): RH1
  • RHD*835A,1136T (DAU3): Prevalence
  • RHD*952T (R318*, RHD*01N.61): Prevalence
  • RHD*952T (R318*, RHD*01N.61): RH1 (adsorption-elution was not performed)
  • RHD*DIIIa-CEVS(4-7)-D (RHD*03N.01): RH1 (adsorption-elution was not performed)
  • RHD*DIIIa-CEVS(4-7)-D (RHD*03N.01): Prevalence
  • RHD*Dpsi (RHD*08N.01): RH1 (adsorption-elution was not performed)
  • RHD*Dpsi (RHD*08N.01): Prevalence
  • standard RHD (RHD*01): RH1
  • standard RHD (RHD*01): Prevalence