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: rs10982445
rs10982445
TNFSF8 ; DELEC1
1.000 0.080 9 114897411 intron variant T/A;C snv
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012
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: 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: rs2075533
rs2075533
TNFSF8 ; DELEC1
0.851 0.160 9 114931351 intron variant G/A;T snv
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012
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: rs3181201
rs3181201
TNFSF8 ; DELEC1
1.000 0.080 9 114901520 intron variant G/C snv 0.56
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012
dbSNP: rs3181360
rs3181360
TNFSF8 ; DELEC1
1.000 0.040 9 114929278 intron variant C/A;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2013 2013
dbSNP: rs3181362
rs3181362
TNFSF8 ; DELEC1
1.000 0.040 9 114905163 intron variant T/C snv 0.21
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2013 2013
dbSNP: rs3181367
rs3181367
TNFSF8 ; DELEC1
1.000 0.080 9 114904398 intron variant G/A snv 0.57
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012
dbSNP: rs3181372
rs3181372
TNFSF8 ; DELEC1
1.000 0.080 9 114903155 3 prime UTR variant A/G snv 0.58
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012
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: rs5003740
rs5003740
TNFSF8 ; DELEC1
1.000 0.080 9 114898321 intron variant G/C;T snv
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012