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: 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: 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: 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
dbSNP: rs11557467
rs11557467
ZPBP2
0.851 0.200 17 39872381 missense variant G/T snv 0.45 0.45
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 2 2012 2012
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: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.010 1.000 1 2013 2013
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: rs12936231
rs12936231
ZPBP2
0.925 0.160 17 39872867 intron variant C/G;T snv
CUI: C0004096
Disease: Asthma
Asthma 		0.720 1.000 3 2011 2019
dbSNP: rs12936231
rs12936231
ZPBP2
0.925 0.160 17 39872867 intron variant C/G;T snv
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 2 2012 2012
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: rs1054609
rs1054609
ZPBP2
0.925 0.160 17 39877024 3 prime UTR variant A/C snv 0.40
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2011 2011
dbSNP: rs1054609
rs1054609
ZPBP2
0.925 0.160 17 39877024 3 prime UTR variant A/C snv 0.40
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012