Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs704840
rs704840
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0027873
Disease:
Neuromyelitis Optica
0.010 GeneticVariation BEFREE Significant associations of rs844648 (OR = 1.67, 95% CI 1.17-2.38, P = 0.005, Pcorr = 0.02) and rs704840 (OR = 1.75, 95% CI 1.17-2.63, P = 0.007, Pcorr = 0.027) with NMOSD occurrence were also observed under the recessive model. 29032462 2017
dbSNP: rs844648
rs844648
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0027873
Disease:
Neuromyelitis Optica
0.010 GeneticVariation BEFREE Significant associations of rs844648 (OR = 1.67, 95% CI 1.17-2.38, P = 0.005, Pcorr = 0.02) and rs704840 (OR = 1.75, 95% CI 1.17-2.63, P = 0.007, Pcorr = 0.027) with NMOSD occurrence were also observed under the recessive model. 29032462 2017
dbSNP: rs1418190
rs1418190
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
0.010 GeneticVariation BEFREE This replication effort confirmed five reported SLE susceptibility loci reaching genome-wide levels of significance (P(meta) <5.00 × 10(-08)): TNFSF4 (rs1418190, odds ratio (OR) = 0.81, P(meta) = 1.08 × 10(-08); rs4916219, OR = 0.80, P(meta )= 7.77 × 10(-09)), IRF8 (rs2934498, OR = 1.25, P(meta) = 4.97 × 10(-09)), miR-146a (rs2431697, OR = 0.69, P(meta) = 1.15 × 10(-22)), CD44 (rs2732547, OR = 0.82, P(meta) = 1.55 × 10(-11)), and TMEM39A (rs12494314, OR = 0.84, P(meta) = 1.01 × 10(-09)). 25890262 2015
dbSNP: rs4916219
rs4916219
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
0.010 GeneticVariation BEFREE This replication effort confirmed five reported SLE susceptibility loci reaching genome-wide levels of significance (P(meta) <5.00 × 10(-08)): TNFSF4 (rs1418190, odds ratio (OR) = 0.81, P(meta) = 1.08 × 10(-08); rs4916219, OR = 0.80, P(meta )= 7.77 × 10(-09)), IRF8 (rs2934498, OR = 1.25, P(meta) = 4.97 × 10(-09)), miR-146a (rs2431697, OR = 0.69, P(meta) = 1.15 × 10(-22)), CD44 (rs2732547, OR = 0.82, P(meta) = 1.55 × 10(-11)), and TMEM39A (rs12494314, OR = 0.84, P(meta) = 1.01 × 10(-09)). 25890262 2015
dbSNP: rs10489265
rs10489265
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0409974
Disease:
Lupus Erythematosus
0.010 GeneticVariation BEFREE The SNPs of TNFSF4 were associated with renal involvement in lupus patients from the Chinese population (P values for rs2205960 and rs10489265 were 0.014 and 0.005 in additive model, resp.). 23936824 2013
dbSNP: rs10489265
rs10489265
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0024131
Disease:
Lupus Vulgaris
0.010 GeneticVariation BEFREE The SNPs of TNFSF4 were associated with renal involvement in lupus patients from the Chinese population (P values for rs2205960 and rs10489265 were 0.014 and 0.005 in additive model, resp.). 23936824 2013
dbSNP: rs10489265
rs10489265
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0024138
Disease:
Lupus Erythematosus, Discoid
0.010 GeneticVariation BEFREE The SNPs of TNFSF4 were associated with renal involvement in lupus patients from the Chinese population (P values for rs2205960 and rs10489265 were 0.014 and 0.005 in additive model, resp.). 23936824 2013
dbSNP: rs10489265
rs10489265
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0014060
Disease:
Encephalitis, St. Louis
0.010 GeneticVariation BEFREE To replicate the association, two single-nucleotide polymorphisms (SNPs: rs2205960 and rs10489265) were genotyped in 814 SLE patients. 23936824 2013
dbSNP: rs704840
rs704840
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0151449
Disease:
Primary Sjögren's syndrome
0.010 GeneticVariation BEFREE Weak associations were observed when the SNPs in TNFSF4 (rs2205960, rs844648 and rs704840) and FAM167A-BLK (rs7812879, rs2254546 and rs2618479) were directly analyzed or analyzed under dominant model between pSS and controls (all P<0.05). 23635951 2013
dbSNP: rs844644
rs844644
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
0.010 GeneticVariation BEFREE No association was found between the rs844644 and rs844648 polymorphisms and SLE. 22850862 2013
dbSNP: rs844648
rs844648
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0151449
Disease:
Primary Sjögren's syndrome
0.010 GeneticVariation BEFREE Weak associations were observed when the SNPs in TNFSF4 (rs2205960, rs844648 and rs704840) and FAM167A-BLK (rs7812879, rs2254546 and rs2618479) were directly analyzed or analyzed under dominant model between pSS and controls (all P<0.05). 23635951 2013
dbSNP: rs10912580
rs10912580
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE The haplotype analysis showed that haplotype A(rs844648)A(rs10912580) was significantly associated with breast cancer, even after 10,000 permutations for haplotypes in block only (P = 0.0003). 22870213 2012
dbSNP: rs10912580
rs10912580
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0036421
Disease:
Systemic Scleroderma
0.010 GeneticVariation BEFREE Known SLE and SSc TNFSF4 susceptibility variants (rs2205960, rs1234317, rs12039904, rs10912580, and rs844648) were genotyped in 1031 patients with SSc and 1014 controls of French white ancestry. 22422496 2012
dbSNP: rs10912580
rs10912580
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE The haplotype analysis showed that haplotype A(rs844648)A(rs10912580) was significantly associated with breast cancer, even after 10,000 permutations for haplotypes in block only (P = 0.0003). 22870213 2012
dbSNP: rs844648
rs844648
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE The haplotype analysis showed that haplotype A(rs844648)A(rs10912580) was significantly associated with breast cancer, even after 10,000 permutations for haplotypes in block only (P = 0.0003). 22870213 2012
dbSNP: rs844648
rs844648
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE The haplotype analysis showed that haplotype A(rs844648)A(rs10912580) was significantly associated with breast cancer, even after 10,000 permutations for haplotypes in block only (P = 0.0003). 22870213 2012
dbSNP: rs12039904
rs12039904
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0036421
Disease:
Systemic Scleroderma
0.020 GeneticVariation BEFREE Known SLE and SSc TNFSF4 susceptibility variants (rs2205960, rs1234317, rs12039904, rs10912580, and rs844648) were genotyped in 1031 patients with SSc and 1014 controls of French white ancestry. 22422496 2012
dbSNP: rs844648
rs844648
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0036421
Disease:
Systemic Scleroderma
0.020 GeneticVariation BEFREE Known SLE and SSc TNFSF4 susceptibility variants (rs2205960, rs1234317, rs12039904, rs10912580, and rs844648) were genotyped in 1031 patients with SSc and 1014 controls of French white ancestry. 22422496 2012
dbSNP: rs12039904
rs12039904
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0036421
Disease:
Systemic Scleroderma
0.020 GeneticVariation BEFREE A pooled analysis revealed the association of rs1234314 and rs12039904 polymorphisms with SSc (OR 1.15, 95% CI 1.02 to 1.31; OR 1.18, 95% CI 1.08 to 1.29, respectively). 21187296 2011
dbSNP: rs844648
rs844648
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0036421
Disease:
Systemic Scleroderma
0.020 GeneticVariation BEFREE Case-control comparisons revealed a significant association between susceptibility to SSc and the minor alleles at SNPs rs1234314 (OR 1.20, 95% CI 1.04 to 1.4, p(FDR)=0.019), rs2205960 (OR 1.24, 95% CI 1.10 to 1.50, p(FDR)=0.019) and rs844648 (OR 1.16, 95% CI 1.01 to 1.30, p(FDR)=0.032). 19778912 2010
dbSNP: rs1099448
rs1099448
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0200638
Disease:
Eosinophil count procedure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2422345
rs2422345
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
A 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis reveals shared new loci in systemic seropositive rheumatic diseases. 30573655 2019
dbSNP: rs2422345
rs2422345
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0027121
Disease:
Myositis
A 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis reveals shared new loci in systemic seropositive rheumatic diseases. 30573655 2019
dbSNP: rs2422345
rs2422345
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0003873
Disease:
Rheumatoid Arthritis
A 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis reveals shared new loci in systemic seropositive rheumatic diseases. 30573655 2019
dbSNP: rs2422345
rs2422345
Entrez Id: 7292;100506023
Gene Symbol: TNFSF4;LOC100506023
TNFSF4;LOC100506023
CUI: C0036421
Disease:
Systemic Scleroderma
A 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis reveals shared new loci in systemic seropositive rheumatic diseases. 30573655 2019