Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3024498
rs3024498
CUI: C0003864
Disease: Arthritis
Arthritis
0.010 GeneticVariation BEFREE Interestingly, significant differences were detected both in the allele and genotype frequencies of rs3024498 between SLE patients with and without arthritis (P=0.002, P=0.022, respectively).There was significant difference in genotype frequency at rs3024498 between SLE patients with and without malar rash (P=0.040). 29199038

2018

dbSNP: rs3024498
rs3024498
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.010 GeneticVariation BEFREE And, there was significant difference in allele frequency at rs3024498 between SLE patients with and without anti-double-stranded DNA (P=0.032). 29199038

2018

dbSNP: rs3024498
rs3024498
CUI: C0014061
Disease: Tick-Borne Encephalitis
Tick-Borne Encephalitis
0.010 GeneticVariation BEFREE The aim of the present study was to estimate a possible association of the IL28B gene rs8103142 and rs12980275 SNPs and IL10 gene rs1800872, rs3021094, and rs3024498 SNPs with predisposition to TBE in a Russian population. 27068548

2016

dbSNP: rs3024498
rs3024498
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 GeneticVariation BEFREE Interestingly, we have found, majority of the tribal populations have low frequency of VL ('A' of rs3024498); and high frequency of leprosy ('T' of rs1554286), and Behcet's ('A' of rs1518111) associated alleles, whereas these were vice versa in castes. 25941808

2015

dbSNP: rs3024498
rs3024498
CUI: C0023290
Disease: Leishmaniasis, Visceral
Leishmaniasis, Visceral
0.010 GeneticVariation BEFREE Interestingly, we have found, majority of the tribal populations have low frequency of VL ('A' of rs3024498); and high frequency of leprosy ('T' of rs1554286), and Behcet's ('A' of rs1518111) associated alleles, whereas these were vice versa in castes. 25941808

2015

dbSNP: rs3024498
rs3024498
CUI: C0018889
Disease: Helminthiasis
Helminthiasis
0.010 GeneticVariation BEFREE Allele C of marker rs3024498 was negatively associated with helminth infection or its markers. 23273955

2013

dbSNP: rs3024498
rs3024498
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.010 GeneticVariation BEFREE The variant of the TNFA gene at rs3093662, the IL12 gene at rs3213094 and rs3212220 and the IL10 gene at rs3024498 did show a strong indication to be of relevance to the immunity to tuberculosis. 21463712

2011