Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5010528
rs5010528
Entrez Id: 3106;3107
Gene Symbol: HLA-B;HLA-C
HLA-B;HLA-C
CUI: C0014518
Disease:
Toxic Epidermal Necrolysis
0.720 GeneticVariation BEFREE Our study confirmed the association of the rs5010528 SNP in the HLA-C region with susceptibility to developing SJS/TEN in a population from Mozambique, suggesting that it could be a good genomic biomarker for SJS/TEN susceptibility in different sub-Saharan populations. 29762688 2018
dbSNP: rs5010528
rs5010528
Entrez Id: 3106;3107
Gene Symbol: HLA-B;HLA-C
HLA-B;HLA-C
CUI: C0014518
Disease:
Toxic Epidermal Necrolysis
0.720 GeneticVariation BEFREE The most promising signal was seen in SJS/TEN, where rs5010528 ( HLA-C locus) approached genome-wide significance ( P  <   8.5 × 10 -8 ) and was below HLA -wide significance ( P  <   2.5 × 10 -4 ) in the meta-analysis of discovery and replication cohorts [OR 4.84 (95% CI 2.71-8.61)]. rs5010528 is a strong proxy for HLA-C*04:01 carriage: in silico docking showed that two residues (33 and 123) in the B pocket were the most likely nevirapine interactors. 28062682 2017
dbSNP: rs5010528
rs5010528
Entrez Id: 3106;3107
Gene Symbol: HLA-B;HLA-C
HLA-B;HLA-C
CUI: C0014518
Disease:
Toxic Epidermal Necrolysis
G 0.720 GeneticVariation GWASCAT The most promising signal was seen in SJS/TEN, where rs5010528 ( HLA-C locus) approached genome-wide significance ( P  <   8.5 × 10 -8 ) and was below HLA -wide significance ( P  <   2.5 × 10 -4 ) in the meta-analysis of discovery and replication cohorts [OR 4.84 (95% CI 2.71-8.61)]. rs5010528 is a strong proxy for HLA-C*04:01 carriage: in silico docking showed that two residues (33 and 123) in the B pocket were the most likely nevirapine interactors. 28062682 2017