Article
Outliers in RhD membrane integration are explained by variant RH haplotypes. Yu X, Wagner FF, Witter B, Flegel WA. Transfusion, 2006. [Citation]
Annotations by Allele
- apparently standard RHD with unexpected serology: Density
- apparently standard RHD with unexpected serology: Density
- apparently standard RHD with unexpected serology: otherHaplotype
- apparently standard RHD with unexpected serology: Density
- apparently standard RHD with unexpected serology: Density
- apparently standard RHD with unexpected serology: Density
- apparently standard RHD with unexpected serology: otherHaplotype
- apparently standard RHD with unexpected serology: Density
- apparently standard RHD with unexpected serology: Density
- apparently standard RHD with unexpected serology: Density
- apparently standard RHD with unexpected serology: Density
- apparently standard RHD with unexpected serology: Density
- apparently standard RHD with unexpected serology: otherHaplotype
- RHD*1154C (weak D type 2): RH1
- RHD*1154C (weak D type 2): otherHaplotype
- RHD*1154C (weak D type 2): Density
- RHD*1154C (weak D type 2): Density
- 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): Density
- RHD*1154C (weak D type 2): Density
- RHD*1154C (weak D type 2): Density
- RHD*1250C (weak D type 20): Density
- RHD*1250C (weak D type 20): RH1
- RHD*1250C (weak D type 20): Serology
- RHD*1250C (weak D type 20): rhesus
- RHD*1250C (weak D type 20): Density
- RHD*1250C (weak D type 20): otherHaplotype
- RHD*1250C (weak D type 20): Prevalence
- RHD*1250C (weak D type 20): Prevalence
- RHD*329C (DVII): Density
- RHD*329C (DVII): Prevalence
- RHD*329C (DVII): RH1
- RHD*329C (DVII): otherHaplotype
- 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): Density
- RHD*48C,602G,667G,819A (weak D type 4.1, DAR4): Density
- RHD*48C,602G,667G,819A (weak D type 4.1, DAR4): RH1
- RHD*48C,602G,667G,819A (weak D type 4.1, DAR4): AbSpecificity
- RHD*48C,602G,667G,819A (weak D type 4.1, DAR4): Density
- RHD*48C,602G,667G,819A (weak D type 4.1, DAR4): otherHaplotype
- RHD*48C,602G,667G,819A (weak D type 4.1, DAR4): Density
- RHD*48C,602G,667G,819A (weak D type 4.1, DAR4): Prevalence
- RHD*48C,602G,667G,819A (weak D type 4.1, DAR4): Density
- RHD*48C,602G,667G,819A (weak D type 4.1, DAR4): Density
- RHD*48C,602G,667G,819A (weak D type 4.1, DAR4): Density
- RHD*602G,667G,819A (weak D type 4.0, DAR3.01): Density
- RHD*602G,667G,819A (weak D type 4.0, DAR3.01): RH1
- RHD*602G,667G,819A (weak D type 4.0, DAR3.01): Density
- RHD*602G,667G,819A (weak D type 4.0, DAR3.01): Prevalence
- RHD*602G,667G,819A (weak D type 4.0, DAR3.01): RH1
- RHD*602G,667G,819A (weak D type 4.0, DAR3.01): otherHaplotype
- RHD*602G,667G,819A (weak D type 4.0, DAR3.01): AbSpecificity
- RHD*602G,667G,819A (weak D type 4.0, DAR3.01): Density
- RHD*602G,667G,819A (weak D type 4.0, DAR3.01): Prevalence
- RHD*602G,667G,819A (weak D type 4.0, DAR3.01): Density
- RHD*611C (weak D type 19): Density
- RHD*611C (weak D type 19): RH1
- RHD*611C (weak D type 19): Serology
- RHD*611C (weak D type 19): rhesus
- RHD*611C (weak D type 19): Density
- RHD*611C (weak D type 19): otherHaplotype
- RHD*611C (weak D type 19): Prevalence
- RHD*611C (weak D type 19): Prevalence
- RHD*700T (DYU, RHD*29): Density
- RHD*700T (DYU, RHD*29): Prevalence
- RHD*700T (DYU, RHD*29): Density
- RHD*700T (DYU, RHD*29): RH1
- RHD*700T (DYU, RHD*29): otherHaplotype
- RHD*700T (DYU, RHD*29): Prevalence
- RHD*700T (DYU, RHD*29): Serology
- RHD*700T (DYU, RHD*29): rhesus
- RHD*809G (weak D type 1): RH1
- RHD*809G (weak D type 1): otherHaplotype
- RHD*809G (weak D type 1): Density
- RHD*809G (weak D type 1): Density
- RHD*809G (weak D type 1): Prevalence
- RHD*8G (weak D type 3): Prevalence
- standard RHD (RHD*01): Density
- standard RHD (RHD*01): RH1
- standard RHD (RHD*01): Density
- standard RHD (RHD*01): Density