Varaico: Literature-Extracted Genetic Variants

Gene:RHD
Variant:p.V306I
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RHD

NM_016124.6:p.V306I

Associated Papers

Partial D variant with demonstrated risk of D alloimmunization in the Australian Indigenous population.

Palfreyman E et al.

Vox Sanguinis, 2025

Alloanti-D induction in a rare RhD variant (DBT-2) case: Insights from serological and molecular biological testing.

Xu Z et al.

Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2025

First investigation of RH gene polymorphism in patients with sickle cell disease and associated blood donors in Cameroon, Central Africa.

Mbeti JMM et al.

Blood Transfusion = Trasfusione Del Sangue, 2024

Machine learning to optimize automated RH genotyping using whole-exome sequencing data.

Chang TC et al.

Blood Advances, 2024

38522094 (PubMed )
Supplement: BLOODA_ADV-2023-011660-mmc1.xlsx › Rh

Characterization of Novel RHD Allele Variants and Their Implications for Routine Blood Group Diagnostics.

Matzhold EM et al.

Biomedicines, 2024

Transfusion management of Africans with RHD variants in China.

Yin Q et al.

Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 2023

RHD Genotypes in a Chinese Cohort of Pregnant Women.

Zhang J et al.

Frontiers in Genetics, 2021

RH genotyping by nonspecific quantitative next-generation sequencing.

Stef M et al.

Transfusion, 2020

Genomic characterization of the RH locus detects complex and novel structural variation in multi-ethnic cohorts.

Wheeler MM et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2019

29955105 (PubMed )
Supplement: NIHMS969264-supplement-Supplementary___Appendix__online_only_material__etc__.pdf

Whole-exome sequencing for RH genotyping and alloimmunization risk in children with sickle cell anemia.

Chou ST et al.

Blood Advances, 2017

A D+ blood donor with a novel RHD*D-CE(5-6)-D gene variant exhibits the low-frequency antigen RH23 (D(W) ) characteristic of the partial DVa phenotype.

Lopez GH et al.

Transfusion, 2016

New RHD variant alleles.

Garcia F et al.

Transfusion, 2015

Partial D phenotypes and genotypes in the Chinese population.

Ye L et al.

Transfusion, 2012

Overcoming methodical limits of standard RHD genotyping by next-generation sequencing.

Stabentheiner S et al.

Vox Sanguinis, 2011

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