Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4997052
rs4997052
HLA-B ; MIR6891
0.010 GeneticVariation BEFREE The novel variant rs4997052 identified in our study can explain another approximately 0.66% of the phenotypic variances of NOA. 30502936

2019