×
Entrez Id:
23327
Gene Symbol:
NEDD4L
NEDD4L
Asthma
0.110
GeneticVariation
GWASDB
A second-generation genomewide screen for asthma-susceptibility alleles in a founder population.
11022011
2000
×
Entrez Id:
3075
Gene Symbol:
CFH
CFH
Age related macular degeneration
0.500
GeneticVariation
GWASDB
The CFH gene is located on chromosome 1 in a region repeatedly linked to AMD in family-based studies.
15761122
2005
×
Entrez Id:
9966
Gene Symbol:
TNFSF15
TNFSF15
Crohn Disease
0.200
GeneticVariation
GWASDB
Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease.
16221758
2005
×
Entrez Id:
944
Gene Symbol:
TNFSF8
TNFSF8
Crohn Disease
0.100
GeneticVariation
GWASDB
Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease.
16221758
2005
×
Entrez Id:
50514
Gene Symbol:
DELEC1
DELEC1
Crohn Disease
0.100
GeneticVariation
GWASDB
Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease.
16221758
2005
×
Entrez Id:
64127
Gene Symbol:
NOD2
NOD2
Crohn Disease
1.000
GeneticVariation
GWASDB
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
17068223
2006
×
Entrez Id:
149233
Gene Symbol:
IL23R
IL23R
Crohn Disease
0.700
GeneticVariation
GWASDB
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
17068223
2006
×
Entrez Id:
387715
Gene Symbol:
ARMS2
ARMS2
Age related macular degeneration
0.700
GeneticVariation
GWASDB
HTRA1 promoter polymorphism in wet age-related macular degeneration.
17053108
2006
×
Entrez Id:
149233
Gene Symbol:
IL23R
IL23R
Inflammatory Bowel Diseases
0.500
GeneticVariation
GWASDB
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
17068223
2006
×
Entrez Id:
64127
Gene Symbol:
NOD2
NOD2
Inflammatory Bowel Diseases
0.500
GeneticVariation
GWASDB
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
17068223
2006
×
Entrez Id:
440823
Gene Symbol:
MIAT
MIAT
Myocardial Infarction
0.500
GeneticVariation
GWASDB
These results indicate that the altered expression of MIAT by the SNP may play some role in the pathogenesis of MI .
17066261
2006
×
Entrez Id:
5654
Gene Symbol:
HTRA1
HTRA1
Age related macular degeneration
0.500
GeneticVariation
GWASDB
Here we report that a single-nucleotide polymorphism in the promoter region of HTRA1 , a serine protease gene on chromosome 10q26, is a major genetic risk factor for wet AMD .
17053108
2006
×
Entrez Id:
6239
Gene Symbol:
RREB1
RREB1
Parkinson Disease
0.110
GeneticVariation
GWASDB
Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.
17052657
2006
C1orf141
Crohn Disease
0.100
GeneticVariation
GWASDB
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
17068223
2006
C1orf141
Inflammatory Bowel Diseases
0.100
GeneticVariation
GWASDB
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
17068223
2006
×
Entrez Id:
441250
Gene Symbol:
TYW1B
TYW1B
Parkinson Disease
0.100
GeneticVariation
GWASDB
Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.
17052657
2006
×
Entrez Id:
9811
Gene Symbol:
CTIF
CTIF
Parkinson Disease
0.100
GeneticVariation
GWASDB
Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.
17052657
2006
×
Entrez Id:
64215
Gene Symbol:
DNAJC1
DNAJC1
Parkinson Disease
0.100
GeneticVariation
GWASDB
Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.
17052657
2006
ADAMTSL1
Parkinson Disease
0.100
GeneticVariation
GWASDB
Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.
17052657
2006
×
Entrez Id:
440279
Gene Symbol:
UNC13C
UNC13C
Parkinson Disease
0.100
GeneticVariation
GWASDB
Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.
17052657
2006
DPY19L2P3
Parkinson Disease
0.100
GeneticVariation
GWASDB
Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.
17052657
2006
×
Entrez Id:
374491
Gene Symbol:
TPTE2P6
TPTE2P6
Parkinson Disease
0.100
GeneticVariation
GWASDB
Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.
17052657
2006
×
Entrez Id:
29119
Gene Symbol:
CTNNA3
CTNNA3
Parkinson Disease
0.100
GeneticVariation
GWASDB
Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.
17052657
2006
×
Entrez Id:
55529
Gene Symbol:
PIP4P2
PIP4P2
Parkinson Disease
0.100
GeneticVariation
GWASDB
Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.
17052657
2006
×
Entrez Id:
9722
Gene Symbol:
NOS1AP
NOS1AP
QT interval feature (observable entity)
0.100
GeneticVariation
GWASDB
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization.
16648850
2006