Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs75853687
rs75853687
LINC01847
A 0.700 GeneticVariation GWASCAT A locus on chromosome 5 shows African ancestry-limited association with alloimmunization in sickle cell disease. 30578281

2018
dbSNP: rs67072384
rs67072384
ARAP1
T 0.700 GeneticVariation GWASCAT A Genome-Wide Screen for Large-Effect Alloimmunization Susceptibility Loci among Red Blood Cell Transfusion Recipients with Sickle Cell Disease. 25670933

2014
dbSNP: rs202229101
rs202229101
GP9
0.010 GeneticVariation BEFREE The NM_000174.4:c.368T allele (rs202229101) has a minor allele frequency of 0.0002, and was not detected in 120 French subjects (families with fetal and neonatal alloimmune thrombocytopenia [FNAIT]), suggesting that it is rarely implicated in alloimmunization. 28561420

2017