Source: GWASCAT

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: rs1250567
rs1250567
ZMIZ1
0.776 0.080 10 79286508 intron variant T/C snv 0.56
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 1 2019 2019
dbSNP: rs1250567
rs1250567
ZMIZ1
0.776 0.080 10 79286508 intron variant T/C snv 0.56
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine 		0.700 1.000 1 2019 2019
dbSNP: rs1250550
rs1250550
ZMIZ1
0.851 0.240 10 79300560 intron variant C/A snv 0.27
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2013 2013
dbSNP: rs1250563
rs1250563
ZMIZ1
0.724 0.240 10 79287626 intron variant G/C snv 0.24
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2015 2015
dbSNP: rs1250573
rs1250573
ZMIZ1
0.827 0.120 10 79282718 intron variant G/A snv 0.23
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs1250563
rs1250563
ZMIZ1
0.724 0.240 10 79287626 intron variant G/C snv 0.24
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2015 2015
dbSNP: rs1250563
rs1250563
ZMIZ1
0.724 0.240 10 79287626 intron variant G/C snv 0.24
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2015 2015
dbSNP: rs1250563
rs1250563
ZMIZ1
0.724 0.240 10 79287626 intron variant G/C snv 0.24
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2015 2015
dbSNP: rs1250563
rs1250563
ZMIZ1
0.724 0.240 10 79287626 intron variant G/C snv 0.24
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2015 2015
dbSNP: rs1250563
rs1250563
ZMIZ1
0.724 0.240 10 79287626 intron variant G/C snv 0.24
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis 		0.700 1.000 1 2015 2015
dbSNP: rs7916441
rs7916441
ZMIZ1
10 79165820 intron variant G/C snv 0.39
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2010 2019
dbSNP: rs1658319
rs1658319
ZMIZ1
10 79165257 intron variant T/C snv 0.81
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1815314
rs1815314
ZMIZ1
10 79169036 intron variant G/A;C;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2014 2014
dbSNP: rs779933
rs779933
ZMIZ1
10 79158760 intron variant G/A snv 0.36
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2015 2015
dbSNP: rs780151
rs780151
ZMIZ1
10 79171724 intron variant G/A snv 0.32
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2013 2013
dbSNP: rs704010
rs704010
ZMIZ1
0.851 0.080 10 79081391 intron variant T/C snv 0.71
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.720 1.000 4 2010 2017
dbSNP: rs1268974
rs1268974
ZMIZ1
1.000 0.080 10 79092621 intron variant A/G snv 0.65
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs1250552
rs1250552
ZMIZ1
0.882 0.200 10 79298270 intron variant A/C;G snv
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.800 1.000 2 2010 2011
dbSNP: rs1250557
rs1250557
ZMIZ1
1.000 0.080 10 79306017 intron variant G/T snv 0.63
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.700 1.000 1 2016 2016
dbSNP: rs1250563
rs1250563
ZMIZ1
0.724 0.240 10 79287626 intron variant G/C snv 0.24
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.700 1.000 1 2015 2015
dbSNP: rs1250573
rs1250573
ZMIZ1
0.827 0.120 10 79282718 intron variant G/A snv 0.23
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs1250567
rs1250567
ZMIZ1
0.776 0.080 10 79286508 intron variant T/C snv 0.56
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2019 2019
dbSNP: rs1250567
rs1250567
ZMIZ1
0.776 0.080 10 79286508 intron variant T/C snv 0.56
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2019 2019
dbSNP: rs1250567
rs1250567
ZMIZ1
0.776 0.080 10 79286508 intron variant T/C snv 0.56
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2019 2019
dbSNP: rs1250567
rs1250567
ZMIZ1
0.776 0.080 10 79286508 intron variant T/C snv 0.56
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2019 2019