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Article

Molecular basis of weak D phenotypes. Wagner FF, Gassner C, Müller TH, Schönitzer D, Schunter F, Flegel WA. Blood, 1999. [Citation]

Annotations by Allele

  • RHD*1016A (weak D type 7): RH1
  • RHD*1016A (weak D type 7): otherHaplotype
  • RHD*1016A (weak D type 7): Prevalence
  • RHD*1016A (weak D type 7): Prevalence
  • RHD*1154C (weak D type 2): RH1
  • RHD*1154C (weak D type 2): Prevalence
  • RHD*1154C (weak D type 2): Prevalence
  • RHD*1154C (weak D type 2): otherHaplotype (haplotype given, not complete phenotype)
  • RHD*1177C (weak D type 10): RH1
  • RHD*1177C (weak D type 10): Prevalence
  • RHD*1177C (weak D type 10): Prevalence
  • RHD*1177C (weak D type 10): otherHaplotype
  • RHD*29A (weak D type 6): Prevalence
  • RHD*29A (weak D type 6): Prevalence
  • RHD*29A (weak D type 6): otherHaplotype
  • RHD*29A (weak D type 6): RH1
  • RHD*446A (weak D type 5): RH1
  • RHD*446A (weak D type 5): Prevalence
  • RHD*446A (weak D type 5): otherHaplotype (haplotype given, not complete phenotype)
  • RHD*446A (weak D type 5): Prevalence
  • RHD*48C,602G,667G,819A (weak D type 4.1, DAR4): Prevalence
  • RHD*48C,602G,667G,819A (weak D type 4.1, DAR4): otherHaplotype (haplotype given, not complete phenotype)
  • RHD*48C,602G,667G,819A (weak D type 4.1, DAR4): RH1
  • RHD*544A,594T,602G (weak D type 14): otherHaplotype
  • RHD*544A,594T,602G (weak D type 14): Prevalence
  • RHD*544A,594T,602G (weak D type 14): RH1
  • RHD*602G,667G,819A (weak D type 4.0, DAR3.01): RH1
  • RHD*602G,667G,819A (weak D type 4.0, DAR3.01): otherHaplotype (haplotype given, not complete phenotype)
  • RHD*602G,667G,819A (weak D type 4.0, DAR3.01): Prevalence
  • RHD*658C (weak D type 16): RH1
  • RHD*658C (weak D type 16): otherHaplotype (haplotype given, not complete phenotype)
  • RHD*658C (weak D type 16): Prevalence
  • RHD*658C (weak D type 16): Prevalence
  • RHD*809G (weak D type 1): otherHaplotype (haplotype given, not complete phenotype)
  • RHD*809G (weak D type 1): RH1
  • RHD*809G (weak D type 1): Prevalence
  • RHD*809G (weak D type 1): Prevalence
  • RHD*826C (weak D type 13): RH1
  • RHD*826C (weak D type 13): otherHaplotype (at least 2 samples; haplotype given, not complete phenotype)
  • RHD*826C (weak D type 13): Prevalence
  • RHD*830A (weak D type 12): RH1
  • RHD*830A (weak D type 12): Prevalence
  • RHD*830A (weak D type 12): Prevalence
  • RHD*830A (weak D type 12): otherHaplotype
  • RHD*845A (weak partial D type 15): Prevalence
  • RHD*845A (weak partial D type 15): otherHaplotype (at least 2 samples; haplotype given, not complete phenotype)
  • RHD*845A (weak partial D type 15): RH1
  • RHD*848T (DHMi, RHD*19): Prevalence
  • RHD*848T (DHMi, RHD*19): RH1
  • RHD*848T (DHMi, RHD*19): otherHaplotype (haplotype given, not complete phenotype)
  • RHD*848T (DHMi, RHD*19): Prevalence
  • RHD*880C (weak D type 9): RH1
  • RHD*880C (weak D type 9): Prevalence
  • RHD*880C (weak D type 9): Prevalence
  • RHD*880C (weak D type 9): otherHaplotype (at least 2 samples; haplotype given, not complete phenotype)
  • RHD*885T (weak partial D type 11): RH1
  • RHD*885T (weak partial D type 11): Prevalence
  • RHD*885T (weak partial D type 11): Prevalence
  • RHD*885T (weak partial D type 11): otherHaplotype
  • RHD*8G (weak D type 3): otherHaplotype (haplotype given, not complete phenotype)
  • RHD*8G (weak D type 3): RH1
  • RHD*8G (weak D type 3): Prevalence
  • RHD*8G (weak D type 3): Prevalence
  • RHD*919A (weak D type 8): Prevalence
  • RHD*919A (weak D type 8): Prevalence
  • RHD*919A (weak D type 8): otherHaplotype
  • RHD*919A (weak D type 8): RH1
  • RHD*D-CE(6-9)-D (DIV type 3): RH1
  • RHD*D-CE(6-9)-D (DIV type 3): Prevalence
  • RHD*D-CE(6-9)-D (DIV type 3): Prevalence
  • RHD*D-CE(6-9)-D (DIV type 3): otherHaplotype (haplotype given, not complete phenotype)
  • weak D type 4 - partly characterized or subtypes not separated: Prevalence