NKX2-3, NK2 homeobox 3, 159296

N. diseases: 22; N. variants: 4
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11190140
rs11190140
0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.810 1.000 2 2008 2014
dbSNP: rs11190140
rs11190140
0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
Digestive System Diseases 0.800 1.000 1 2010 2010
dbSNP: rs11190141
rs11190141
1.000 0.040 10 99532633 upstream gene variant C/T snv 0.40
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.800 1.000 1 2012 2012
dbSNP: rs10883371
rs10883371
1.000 0.040 10 99532698 upstream gene variant C/A snv 0.54
CUI: C0566602
Disease: Primary sclerosing cholangitis
Primary sclerosing cholangitis
Digestive System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs11190140
rs11190140
0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
Immune System Diseases; Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs11190140
rs11190140
0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs11190141
rs11190141
1.000 0.040 10 99532633 upstream gene variant C/T snv 0.40
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs11190141
rs11190141
1.000 0.040 10 99532633 upstream gene variant C/T snv 0.40
CUI: C0750880
Disease: Monocyte count result
Monocyte count result
0.700 1.000 1 2016 2016
dbSNP: rs11190140
rs11190140
0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
Digestive System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs11190140
rs11190140
0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55
CUI: C0022104
Disease: Irritable Bowel Syndrome
Irritable Bowel Syndrome
Digestive System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs888208
rs888208
0.882 0.080 10 99536106 3 prime UTR variant A/G snv 0.25
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
Digestive System Diseases; Nutritional and Metabolic Diseases 0.010 1.000 1 2009 2009
dbSNP: rs888208
rs888208
0.882 0.080 10 99536106 3 prime UTR variant A/G snv 0.25
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
Digestive System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs888208
rs888208
0.882 0.080 10 99536106 3 prime UTR variant A/G snv 0.25
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.010 1.000 1 2011 2011