Article
How do we identify RHD variants using a practical molecular approach? Arnoni CP, Latini FR, Muniz JG, Gazito D, Person Rde M, de Paula Vendrame TA, Barreto JA, Castilho L. Transfusion, 2014. [Citation]
Annotations by Allele
- RHD*1063A (DNB, RHD*25): Prevalence
- RHD*1063A (DNB, RHD*25): otherHaplotype (haplotype listed, not complete phenotype)
- RHD*1136T (DAU0): otherHaplotype (haplotype listed, not complete phenotype)
- RHD*1136T (DAU0): Prevalence
- RHD*1154C (weak D type 2): otherHaplotype (haplotype given, not complete phenotype)
- RHD*1154C (weak D type 2): Prevalence
- RHD*161C (DMH, RHD*23): otherHaplotype (haplotype listed, not complete phenotype)
- RHD*161C (DMH, RHD*23): Prevalence
- RHD*186T,410T,455C,1048C (DIVa): otherHaplotype (haplotype listed, not complete phenotype)
- RHD*186T,410T,455C,1048C (DIVa): Prevalence
- RHD*19T (weak D type 18): otherHaplotype (haplotype listed, not complete phenotype)
- RHD*19T (weak D type 18): Prevalence
- RHD*329C (DVII): otherHaplotype (haplotype listed, not complete phenotype)
- RHD*329C (DVII): Prevalence
- RHD*410T,455C,602G,667G,819A (DIII type 6): otherHaplotype (haplotype listed, not complete phenotype)
- RHD*410T,455C,602G,667G,819A (DIII type 6): 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): Prevalence
- RHD*509C,667G,1132G (DOL2, RHD*12.02): otherHaplotype (haplotype listed, not complete phenotype)
- RHD*509C,667G,1132G (DOL2, RHD*12.02): Prevalence
- RHD*602G,667G,1025C (weak D type 4.2.0, DAR1.00): otherHaplotype (haplotype listed, not complete phenotype)
- RHD*602G,667G,1025C (weak D type 4.2.0, DAR1.00): Prevalence
- RHD*602G,667G,744T,957A,1025C (weak D type 4.2.2, DAR1.02): Prevalence
- RHD*602G,667G,744T,957A,1025C (weak D type 4.2.2, DAR1.02): otherHaplotype (haplotype listed, not complete phenotype)
- RHD*602G,667G,819A (weak D type 4.0, DAR3.01): otherHaplotype (haplotype listed, not complete phenotype)
- RHD*602G,667G,819A (weak D type 4.0, DAR3.01): Prevalence
- RHD*667G,697C (DV type 1, Kou): otherHaplotype
- RHD*667G,697C (DV type 1, Kou): Prevalence
- RHD*667G,697C,1136T (DAU5): otherHaplotype (haplotype listed, not complete phenotype)
- RHD*667G,697C,1136T (DAU5): Prevalence
- RHD*689T,1136T (DAU1): otherHaplotype (haplotype listed, not complete phenotype)
- RHD*689T,1136T (DAU1): Prevalence
- RHD*809G (weak D type 1): otherHaplotype (haplotype given, not complete phenotype)
- RHD*809G (weak D type 1): Prevalence
- RHD*833A (weak D type 38): otherHaplotype (haplotype given, not complete phenotype)
- RHD*833A (weak D type 38): Prevalence
- RHD*8G (weak D type 3): Prevalence
- RHD*8G (weak D type 3): otherHaplotype (haplotype given, not complete phenotype)
- RHD*998A,1136T (DAU6): Prevalence
- RHD*998A,1136T (DAU6): otherHaplotype (haplotype listed, not complete phenotype)
- RHD*D-CE(5)-D (DV type 2, Hus): Prevalence
- RHD*D-CE(5)-D (DV type 2, Hus): otherHaplotype (haplotype listed, not complete phenotype)
- RHD*Dpsi (RHD*08N.01): otherHaplotype