Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs946263
rs946263
CUI: C0004096
Disease: Asthma
Asthma 		A 0.700 GeneticVariation GWASDB A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. 11022011

2000
dbSNP: rs545854
rs545854
CUI: C0004096
Disease: Asthma
Asthma 		G 0.700 GeneticVariation GWASDB A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. 11022011

2000
dbSNP: rs4950929
rs4950929
CUI: C0004096
Disease: Asthma
Asthma 		A 0.700 GeneticVariation GWASDB A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. 11022011

2000
dbSNP: rs4436440
rs4436440
CUI: C0004096
Disease: Asthma
Asthma 		T 0.700 GeneticVariation GWASDB A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. 11022011

2000
dbSNP: rs2538026
rs2538026
CUI: C0004096
Disease: Asthma
Asthma 		T 0.700 GeneticVariation GWASDB A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. 11022011

2000
dbSNP: rs2153101
rs2153101
CUI: C0004096
Disease: Asthma
Asthma 		T 0.700 GeneticVariation GWASDB A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. 11022011

2000
dbSNP: rs17064520
rs17064520
NEDD4L
CUI: C0004096
Disease: Asthma
Asthma 		C 0.700 GeneticVariation GWASDB A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. 11022011

2000
dbSNP: rs1229598
rs1229598
CUI: C0004096
Disease: Asthma
Asthma 		C 0.700 GeneticVariation GWASDB A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. 11022011

2000
dbSNP: rs10800812
rs10800812
CUI: C0004096
Disease: Asthma
Asthma 		T 0.700 GeneticVariation GWASDB A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. 11022011

2000
dbSNP: rs3810936
rs3810936
TNFSF15
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.850 GeneticVariation GWASDB Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. 16221758

2005
dbSNP: rs7848647
rs7848647
TNFSF15
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.840 GeneticVariation GWASDB Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. 16221758

2005
dbSNP: rs7869487
rs7869487
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.830 GeneticVariation GWASDB Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. 16221758

2005
dbSNP: rs6478109
rs6478109
TNFSF15
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.830 GeneticVariation GWASDB Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. 16221758

2005
dbSNP: rs6478106
rs6478106
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.820 GeneticVariation GWASDB Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. 16221758

2005
dbSNP: rs380390
rs380390
CFH
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		C 0.810 GeneticVariation GWASDB Complement factor H polymorphism in age-related macular degeneration. 15761122

2005
dbSNP: rs6478108
rs6478108
TNFSF15
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.760 GeneticVariation GWASDB Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. 16221758

2005
dbSNP: rs4979462
rs4979462
TNFSF15
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.720 GeneticVariation GWASDB Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. 16221758

2005
dbSNP: rs4574921
rs4574921
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASDB Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. 16221758

2005
dbSNP: rs4372078
rs4372078
TNFSF15
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASDB Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. 16221758

2005
dbSNP: rs3789882
rs3789882
TNFSF8 ; DELEC1
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASDB Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. 16221758

2005
dbSNP: rs3789879
rs3789879
TNFSF8 ; DELEC1
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASDB Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. 16221758

2005
dbSNP: rs2974
rs2974
TNFSF8 ; DELEC1
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASDB Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. 16221758

2005
dbSNP: rs2295800
rs2295800
TNFSF8 ; DELEC1
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASDB Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. 16221758

2005
dbSNP: rs1885383
rs1885383
TNFSF8 ; DELEC1
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASDB Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. 16221758

2005
dbSNP: rs16931910
rs16931910
DELEC1
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASDB Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. 16221758

2005