Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2858870
rs2858870
Nodular Sclerosis Classical Hodgkin Lymphoma
C 0.710 GeneticVariation GWASCAT These SNPs are found on 2 haplotypes associated with NSHL risk (rs204999-rs9268528-rs9268542-rs6903608-rs2858870; AGGCT, OR = 1.7, P = 1.71 × 10(-6); GAATC, OR = 0.4, P = 1.16 × 10(-4)). 22086417

2012

dbSNP: rs2858870
rs2858870
Nodular Sclerosis Classical Hodgkin Lymphoma
0.710 GeneticVariation BEFREE These SNPs are found on 2 haplotypes associated with NSHL risk (rs204999-rs9268528-rs9268542-rs6903608-rs2858870; AGGCT, OR = 1.7, P = 1.71 × 10(-6); GAATC, OR = 0.4, P = 1.16 × 10(-4)). 22086417

2012

dbSNP: rs2858870
rs2858870
Nodular Sclerosis Classical Hodgkin Lymphoma
T 0.710 GeneticVariation GWASCAT These SNPs are found on 2 haplotypes associated with NSHL risk (rs204999-rs9268528-rs9268542-rs6903608-rs2858870; AGGCT, OR = 1.7, P = 1.71 × 10(-6); GAATC, OR = 0.4, P = 1.16 × 10(-4)). 22086417

2012

dbSNP: rs2858870
rs2858870
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 GeneticVariation GWASDB Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC. 20526339

2010

dbSNP: rs2858870
rs2858870
Diabetes Mellitus, Insulin-Dependent
0.700 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545

2007

dbSNP: rs2858870
rs2858870
CUI: C0014038
Disease: Encephalitis
Encephalitis
0.010 GeneticVariation BEFREE Anti-LGI1 encephalitis was highly associated with 27 single-nucleotide polymorphisms (SNPs) in the HLA-II region (leading SNP rs2858870 p = 1.22 × 10<sup>-17</sup> , OR = 13.66 [7.50-24.87]). 29572931

2018