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: rs4795397
rs4795397
ZPBP2
0.925 0.160 17 39867492 upstream gene variant A/G snv 0.38
CUI: C0004096
Disease: Asthma
Asthma 		0.710 1.000 2 2012 2017
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: rs11557466
rs11557466
ZPBP2
0.925 0.160 17 39868373 synonymous variant C/T snv 0.40 0.36
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2013 2013
dbSNP: rs11557466
rs11557466
ZPBP2
0.925 0.160 17 39868373 synonymous variant C/T snv 0.40 0.36
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2011 2011
dbSNP: rs11557466
rs11557466
ZPBP2
0.925 0.160 17 39868373 synonymous variant C/T snv 0.40 0.36
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012
dbSNP: rs11078925
rs11078925
ZPBP2
0.925 0.160 17 39868955 intron variant T/C snv 0.36
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2013 2013
dbSNP: rs11078925
rs11078925
ZPBP2
0.925 0.160 17 39868955 intron variant T/C snv 0.36
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2011 2011
dbSNP: rs11078925
rs11078925
ZPBP2
0.925 0.160 17 39868955 intron variant T/C snv 0.36
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012
dbSNP: rs12150079
rs12150079
ZPBP2
0.807 0.280 17 39869164 intron variant G/A snv 0.24
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 2 2010 2011
dbSNP: rs12150079
rs12150079
ZPBP2
0.807 0.280 17 39869164 intron variant G/A snv 0.24
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.010 1.000 1 2018 2018
dbSNP: rs12150079
rs12150079
ZPBP2
0.807 0.280 17 39869164 intron variant G/A snv 0.24
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2018 2018
dbSNP: rs12150079
rs12150079
ZPBP2
0.807 0.280 17 39869164 intron variant G/A snv 0.24
CUI: C0014378
Disease: Enterovirus Infections
Enterovirus Infections 		0.010 1.000 1 2015 2015
dbSNP: rs12150079
rs12150079
ZPBP2
0.807 0.280 17 39869164 intron variant G/A snv 0.24
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.010 1.000 1 2018 2018
dbSNP: rs12150079
rs12150079
ZPBP2
0.807 0.280 17 39869164 intron variant G/A snv 0.24
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.010 1.000 1 2015 2015
dbSNP: rs12150079
rs12150079
ZPBP2
0.807 0.280 17 39869164 intron variant G/A snv 0.24
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		0.010 1.000 1 2018 2018
dbSNP: rs12150079
rs12150079
ZPBP2
0.807 0.280 17 39869164 intron variant G/A snv 0.24
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.010 < 0.001 1 2018 2018
dbSNP: rs12150079
rs12150079
ZPBP2
0.807 0.280 17 39869164 intron variant G/A snv 0.24
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2018 2018
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: 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: rs189660050
rs189660050
ZPBP2
1.000 0.040 17 39870781 missense variant C/T snv 2.8E-05 1.9E-04
CUI: C0740394
Disease: Hyperuricemia
Hyperuricemia 		0.010 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: 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: rs11557467
rs11557467
ZPBP2
0.851 0.200 17 39872381 missense variant G/T snv 0.45 0.45
CUI: C0004096
Disease: Asthma
Asthma 		0.710 1.000 2 2010 2011