Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs35736272
rs35736272
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007

2016

dbSNP: rs59716545
rs59716545
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
T 0.700 GeneticVariation GWASCAT Genetic influences on susceptibility to rheumatoid arthritis in African-Americans. 30423114

2019

dbSNP: rs35736272
rs35736272
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007

2016

dbSNP: rs10852936
rs10852936
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.010 GeneticVariation BEFREE We confirmed four known psoriasis susceptibility loci (IL12B, IFIH1, ERAP1 and RNF114; 2.30 × 10(-20)≤P≤2.41 × 10(-7)) and identified three new susceptibility loci: 4q24 (NFKB1) at rs1020760 (P=2.19 × 10(-8)), 12p13.3 (CD27-LAG3) at rs758739 (P=4.08 × 10(-8)) and 17q12 (IKZF3) at rs10852936 (P=1.96 × 10(-8)). 25006012

2014

dbSNP: rs12150079
rs12150079
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 GeneticVariation BEFREE The stratified analysis showed that the associations of rs8076131 and rs12150079 with cervical cancer risk were statistically significant in subgroups of older menarche age (>16 years), more parities (≥2), nonsmokers, and having no family cancer history, but the test results for subgroup heterogeneity were not significant. 30096453

2018

dbSNP: rs9903250
rs9903250
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 GeneticVariation GWASDB Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants. 22936693

2012

dbSNP: rs9891174
rs9891174
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012

dbSNP: rs4795397
rs4795397
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012

dbSNP: rs36095411
rs36095411
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012

dbSNP: rs35736272
rs35736272
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012

dbSNP: rs34189114
rs34189114
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012

dbSNP: rs13380815
rs13380815
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012

dbSNP: rs12936231
rs12936231
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 GeneticVariation GWASDB Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants. 22936693

2012

dbSNP: rs12936231
rs12936231
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012

dbSNP: rs12709365
rs12709365
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012

dbSNP: rs11870965
rs11870965
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012

dbSNP: rs11650661
rs11650661
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012

dbSNP: rs11557467
rs11557467
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012

dbSNP: rs11557467
rs11557467
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 GeneticVariation GWASDB Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants. 22936693

2012

dbSNP: rs11557466
rs11557466
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012

dbSNP: rs11078925
rs11078925
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012

dbSNP: rs10852936
rs10852936
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012

dbSNP: rs10852935
rs10852935
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012

dbSNP: rs1054609
rs1054609
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012

dbSNP: rs12150079
rs12150079
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.010 GeneticVariation BEFREE We found that the G allele of rs8076131 and the A allele of rs12150079 in 17q12 region were significantly associated with increased risk of cervical cancer (adjusted OR = 1.15, 95% CI = 1.02-1.30, P = 0.02 for rs8076131; adjusted OR = 1.19, 95% CI = 1.03-1.36, P = 0.02 for rs12150079). 30096453

2018