Article
Variant screening of the RHD gene in a large cohort of subjects with D phenotype ambiguity: report of 17 novel rare alleles. Fichou Y, Le Maréchal C, Bryckaert L, Guerry C, Bénech C, Dupont I, Jamet D, Férec C, Chen JM. Transfusion, 2012. [Citation]
Annotations by Allele
- RHD*1053T,1057_1061delinsTGGAA (DWN, RHD*49): RH1
- RHD*1053T,1057_1061delinsTGGAA (DWN, RHD*49): Prevalence
- RHD*1175C: RH1
- RHD*1175C: Prevalence
- RHD*1190G (weak D type 156): RH1
- RHD*1190G (weak D type 156): Prevalence
- RHD*1269C: RH1
- RHD*1269C: Prevalence
- RHD*147G: RH1
- RHD*147G: Prevalence
- RHD*163C (weak D type 130): RH1
- RHD*163C (weak D type 130): Prevalence
- RHD*208T (weak D type 122): RH1
- RHD*208T (weak D type 122): Prevalence
- RHD*213T: RH1
- RHD*213T: Prevalence
- RHD*340T,579A,1136T (DAU8): RH1
- RHD*340T,579A,1136T (DAU8): Prevalence
- RHD*365G (weak D type 153): RH1
- RHD*365G (weak D type 153): Prevalence
- RHD*535C,1136T (DAU9): RH1
- RHD*535C,1136T (DAU9): Prevalence
- RHD*538A: RH1
- RHD*538A: Prevalence
- RHD*579A,739A,1136T (DAU10): RH1
- RHD*579A,739A,1136T (DAU10): Prevalence
- RHD*602G,667G,819A,919A: RH1
- RHD*602G,667G,819A,919A: Prevalence
- RHD*626T: RH1
- RHD*626T: Prevalence
- RHD*667G,833T: Prevalence
- RHD*667G,833T: RH1
- RHD*712C,809G: RH1
- RHD*712C,809G: Prevalence