Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10800812
rs10800812 		1.000 0.080 1 202086810 intergenic variant A/G snv 0.77
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2000 2000
dbSNP: rs1229598
rs1229598 		1.000 0.080 18 56267556 regulatory region variant A/C;G;T snv
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2000 2000
dbSNP: rs17064520
rs17064520
NEDD4L
1.000 0.080 18 58242398 intron variant C/T snv 0.19
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2000 2000
dbSNP: rs2153101
rs2153101 		1.000 0.080 1 203199346 intergenic variant A/T snv 0.84
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2000 2000
dbSNP: rs2538026
rs2538026 		1.000 0.080 18 56261410 intergenic variant A/C;G snv
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2000 2000
dbSNP: rs4436440
rs4436440 		1.000 0.080 1 202082885 TF binding site variant T/A snv 0.80
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2000 2000
dbSNP: rs4950929
rs4950929 		1.000 0.080 1 203190998 upstream gene variant G/T snv 0.84
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2000 2000
dbSNP: rs545854
rs545854 		0.882 0.160 8 10002570 intron variant G/C snv 0.85
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2000 2000
dbSNP: rs946263
rs946263 		1.000 0.080 1 203196253 intergenic variant G/A snv 0.86
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2000 2000
dbSNP: rs10117785
rs10117785
TNFSF15
1.000 0.040 9 114789323 3 prime UTR variant T/A snv 0.34
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2005 2005
dbSNP: rs1322054
rs1322054
TNFSF8 ; DELEC1
1.000 0.040 9 114907019 intron variant A/G snv 0.58
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2005 2005
dbSNP: rs16931910
rs16931910
DELEC1
1.000 0.040 9 114856029 intron variant A/C snv 7.2E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2005 2005
dbSNP: rs1885383
rs1885383
TNFSF8 ; DELEC1
1.000 0.040 9 114917522 intron variant G/A snv 0.21
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2005 2005
dbSNP: rs2295800
rs2295800
TNFSF8 ; DELEC1
1.000 0.040 9 114901931 intron variant T/C snv 0.56
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2005 2005
dbSNP: rs2974
rs2974
TNFSF8 ; DELEC1
1.000 0.040 9 114901892 intron variant T/C snv 0.56
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2005 2005
dbSNP: rs3789879
rs3789879
TNFSF8 ; DELEC1
1.000 0.040 9 114915956 intron variant T/C snv 0.58
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2005 2005
dbSNP: rs3789882
rs3789882
TNFSF8 ; DELEC1
1.000 0.040 9 114907419 intron variant A/T snv 0.22
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2005 2005
dbSNP: rs4372078
rs4372078
TNFSF15
1.000 0.040 9 114801407 intron variant T/G snv 0.78
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2005 2005
dbSNP: rs4574921
rs4574921 		0.882 0.160 9 114776054 upstream gene variant C/T snv 0.80
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2005 2005
dbSNP: rs10489629
rs10489629
IL23R ; C1orf141
0.827 0.240 1 67222666 intron variant T/C snv 0.48
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2006 2006
dbSNP: rs10518765
rs10518765
UNC13C
1.000 0.040 15 54388434 intron variant A/C snv 0.16
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2006 2006
dbSNP: rs10963676
rs10963676
ADAMTSL1
1.000 0.040 9 18622045 intron variant T/C;G snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2006 2006
dbSNP: rs1105267
rs1105267 		1.000 0.040 13 20365097 intergenic variant G/A snv 0.54
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2006 2006
dbSNP: rs12069733
rs12069733 		1.000 0.040 1 43475837 TF binding site variant G/A snv 0.37
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2006 2006
dbSNP: rs12364577
rs12364577
LOC440040
1.000 0.040 11 49685809 intron variant A/C snv 0.35
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2006 2006