Article
RhD variants in Caucasians: consequences for checking clinically relevant alleles. Ansart-Pirenne H, Asso-Bonnet M, Le Pennec PY, Roussel M, Patereau C, Noizat-Pirenne F. Transfusion, 2004. [Citation]
Annotations by Allele
- DAL (DV type 7) - phenotypic description: RH1
- DAL (DV type 7) - phenotypic description: Serology
- DAL (DV type 7) - phenotypic description: Prevalence (samples may overlap with
11452170 ) - DBT - phenotypic description: RH1
- DBT - phenotypic description: Serology
- DBT - phenotypic description: Prevalence
- DFR - phenotypic description: AbSpecificity
- DFR - phenotypic description: Prevalence
- DFR - phenotypic description: RH1
- DFR - phenotypic description: Serology
- DNB - phenotypic description: RH1
- DNB - phenotypic description: Serology
- DNB - phenotypic description: AbSpecificity
- DNB - phenotypic description: Prevalence
- DVa - phenotypic description: AbSpecificity
- DVa - phenotypic description: Serology
- DVa - phenotypic description: Prevalence
- DVa - phenotypic description: RH1
- DVI - phenotypic description: Serology
- DVI - phenotypic description: Prevalence
- DVI - phenotypic description: RH1
- DVI - phenotypic description: AbSpecificity
- DVII - phenotypic description: RH1
- DVII - phenotypic description: Serology
- DVII - phenotypic description: AbSpecificity
- DVII - phenotypic description: Prevalence
- R0Har/DHAR - phenotypic description: RH1
- R0Har/DHAR - phenotypic description: Prevalence
- RHD*1015A (weak D type 39): RH1
- RHD*1015A (weak D type 39): Serology
- RHD*1015A (weak D type 39): rhesus
- RHD*1015A (weak D type 39): Density
- RHD*1015A (weak D type 39): otherHaplotype
- RHD*1015A (weak D type 39): Prevalence
- RHD*1154C (weak D type 2): otherHaplotype (sample count not clear, between 11 and 19)
- RHD*1154C (weak D type 2): Density
- RHD*1154C (weak D type 2): Prevalence
- RHD*1154C (weak D type 2): Density
- RHD*1154C (weak D type 2): RH1
- RHD*1154C (weak D type 2): otherHaplotype (sample count not clear, between 2 and 10)
- RHD*1177C (weak D type 10): RH1
- RHD*1177C (weak D type 10): Density
- RHD*1177C (weak D type 10): otherHaplotype
- RHD*1177C (weak D type 10): Prevalence
- RHD*399T (weak D type 37): Density
- RHD*399T (weak D type 37): otherHaplotype
- RHD*399T (weak D type 37): Prevalence
- RHD*399T (weak D type 37): RH1
- RHD*399T (weak D type 37): Serology
- RHD*399T (weak D type 37): rhesus
- RHD*680C (DBA, RHD*56): Density
- RHD*680C (DBA, RHD*56): otherHaplotype
- RHD*680C (DBA, RHD*56): Prevalence
- RHD*680C (DBA, RHD*56): RH1
- RHD*680C (DBA, RHD*56): Serology
- RHD*680C (DBA, RHD*56): rhesus
- RHD*809G (weak D type 1): otherHaplotype (sample count not clear, between 4 and 28)
- RHD*809G (weak D type 1): otherHaplotype (sample count not clear, between 2 and 26)
- RHD*809G (weak D type 1): Density
- RHD*809G (weak D type 1): Prevalence
- RHD*809G (weak D type 1): Density
- RHD*809G (weak D type 1): RH1
- RHD*809G (weak D type 1): otherHaplotype
- RHD*833A (weak D type 38): otherHaplotype
- RHD*833A (weak D type 38): RH1
- RHD*833A (weak D type 38): Serology
- RHD*833A (weak D type 38): rhesus
- RHD*833A (weak D type 38): Density
- RHD*833A (weak D type 38): Prevalence
- RHD*845A (weak partial D type 15): RH1
- RHD*845A (weak partial D type 15): Density
- RHD*845A (weak partial D type 15): otherHaplotype
- RHD*845A (weak partial D type 15): Prevalence
- RHD*851T (DLO, RHD*36): RH1
- RHD*851T (DLO, RHD*36): Serology
- RHD*851T (DLO, RHD*36): rhesus
- RHD*851T (DLO, RHD*36): Density
- RHD*851T (DLO, RHD*36): Prevalence
- RHD*851T (DLO, RHD*36): otherHaplotype
- RHD*885T (weak partial D type 11): Prevalence
- RHD*885T (weak partial D type 11): RH1
- RHD*885T (weak partial D type 11): otherHaplotype
- RHD*885T (weak partial D type 11): Density
- RHD*8G (weak D type 3): RH1
- RHD*8G (weak D type 3): otherHaplotype
- RHD*8G (weak D type 3): Prevalence
- RHD*8G (weak D type 3): Density
- RHD*919A (weak D type 8): RH1
- RHD*919A (weak D type 8): Density
- RHD*919A (weak D type 8): otherHaplotype
- RHD*919A (weak D type 8): Prevalence