Source: ALL

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: rs11557467
rs11557467
ZPBP2
0.851 0.200 17 39872381 missense variant G/T snv 0.45 0.45
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		0.700 1.000 1 2007 2007
dbSNP: rs11557467
rs11557467
ZPBP2
0.851 0.200 17 39872381 missense variant G/T snv 0.45 0.45
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2013 2013
dbSNP: rs11650661
rs11650661
ZPBP2
1.000 0.080 17 39870033 intron variant A/C;T snv
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012
dbSNP: rs11655198
rs11655198
ZPBP2
1.000 0.080 17 39869916 intron variant C/T snv 0.43
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2016 2016
dbSNP: rs11658278
rs11658278
ZPBP2
1.000 0.080 17 39874911 intron variant T/C snv 0.46
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 1 2018 2018
dbSNP: rs11870965
rs11870965
ZPBP2
0.925 0.160 17 39873952 intron variant T/A snv 0.40
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2013 2013
dbSNP: rs11870965
rs11870965
ZPBP2
0.925 0.160 17 39873952 intron variant T/A snv 0.40
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012
dbSNP: rs11870965
rs11870965
ZPBP2
0.925 0.160 17 39873952 intron variant T/A snv 0.40
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2011 2011
dbSNP: rs12709365
rs12709365
ZPBP2
1.000 0.080 17 39871147 intron variant A/G snv 0.40
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012
dbSNP: rs12936231
rs12936231
ZPBP2
0.925 0.160 17 39872867 intron variant C/G;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2013 2013
dbSNP: rs12939457
rs12939457
ZPBP2
1.000 0.120 17 39875935 intron variant T/C snv 0.38
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		0.700 1.000 1 2018 2018
dbSNP: rs13380815
rs13380815
ZPBP2
1.000 0.080 17 39871330 intron variant A/G snv 0.40
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012
dbSNP: rs34189114
rs34189114
ZPBP2
1.000 0.080 17 39876207 intron variant C/T snv 0.36
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012
dbSNP: rs35736272
rs35736272
ZPBP2
0.807 0.160 17 39876427 intron variant T/C snv 0.35
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016
dbSNP: rs35736272
rs35736272
ZPBP2
0.807 0.160 17 39876427 intron variant T/C snv 0.35
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs35736272
rs35736272
ZPBP2
0.807 0.160 17 39876427 intron variant T/C snv 0.35
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs35736272
rs35736272
ZPBP2
0.807 0.160 17 39876427 intron variant T/C snv 0.35
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs35736272
rs35736272
ZPBP2
0.807 0.160 17 39876427 intron variant T/C snv 0.35
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012
dbSNP: rs35736272
rs35736272
ZPBP2
0.807 0.160 17 39876427 intron variant T/C snv 0.35
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs36095411
rs36095411
ZPBP2
1.000 0.080 17 39875612 intron variant T/A;G snv
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012
dbSNP: rs4795397
rs4795397
ZPBP2
0.925 0.160 17 39867492 upstream gene variant A/G snv 0.38
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012
dbSNP: rs4795397
rs4795397
ZPBP2
0.925 0.160 17 39867492 upstream gene variant A/G snv 0.38
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 1 2015 2015
dbSNP: rs4795397
rs4795397
ZPBP2
0.925 0.160 17 39867492 upstream gene variant A/G snv 0.38
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2013 2013
dbSNP: rs59716545
rs59716545
ZPBP2
1.000 0.120 17 39875604 intron variant T/G snv 0.35
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 1 2019 2019
dbSNP: rs9891174
rs9891174
ZPBP2
1.000 0.080 17 39875549 intron variant T/A snv 0.39
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012