KIAA1109, KIAA1109, 84162

N. diseases: 86; N. variants: 30
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: rs11938795
rs11938795
0.882 0.120 4 122151854 upstream gene variant T/C snv 0.24
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs13119723
rs13119723
0.807 0.280 4 122297158 intron variant A/G snv 0.10
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.800 1.000 1 2010 2010
dbSNP: rs13119723
rs13119723
0.807 0.280 4 122297158 intron variant A/G snv 0.10
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs13119723
rs13119723
0.807 0.280 4 122297158 intron variant A/G snv 0.10
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2010 2010
dbSNP: rs13119723
rs13119723
0.807 0.280 4 122297158 intron variant A/G snv 0.10
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2010 2010
dbSNP: rs13119723
rs13119723
0.807 0.280 4 122297158 intron variant A/G snv 0.10
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases
Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs13151961
rs13151961
0.827 0.200 4 122194347 intron variant A/G snv 0.11
CUI: C0566602
Disease: Primary sclerosing cholangitis
Primary sclerosing cholangitis
Digestive System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs13151961
rs13151961
0.827 0.200 4 122194347 intron variant A/G snv 0.11
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs13151961
rs13151961
0.827 0.200 4 122194347 intron variant A/G snv 0.11
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases
Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs13151961
rs13151961
0.827 0.200 4 122194347 intron variant A/G snv 0.11
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
Digestive System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs13151961
rs13151961
0.827 0.200 4 122194347 intron variant A/G snv 0.11
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
Immune System Diseases; Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs138538714
rs138538714
1.000 0.080 4 122194117 intron variant C/G;T snv
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs4288027
rs4288027
4 122262050 intron variant A/C;G snv 0.13
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases
Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs4288027
rs4288027
4 122262050 intron variant A/C;G snv 0.13
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs4374642
rs4374642
4 122179956 intron variant T/C snv 0.13
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases
Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs4374642
rs4374642
4 122179956 intron variant T/C snv 0.13
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs4505848
rs4505848
0.776 0.400 4 122211337 intron variant A/G snv 0.29
CUI: C0042167
Disease: Uveitis, Posterior
Uveitis, Posterior
Eye Diseases 0.010 1.000 1 2012 2012
dbSNP: rs4505848
rs4505848
0.776 0.400 4 122211337 intron variant A/G snv 0.29
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs4505848
rs4505848
0.776 0.400 4 122211337 intron variant A/G snv 0.29
CUI: C0701807
Disease: Acute anterior uveitis
Acute anterior uveitis
Eye Diseases 0.010 1.000 1 2011 2011
dbSNP: rs4505848
rs4505848
0.776 0.400 4 122211337 intron variant A/G snv 0.29
CUI: C0042164
Disease: Uveitis
Uveitis
Eye Diseases 0.010 1.000 1 2012 2012
dbSNP: rs4505848
rs4505848
0.776 0.400 4 122211337 intron variant A/G snv 0.29
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs4505848
rs4505848
0.776 0.400 4 122211337 intron variant A/G snv 0.29
CUI: C0042165
Disease: Anterior uveitis
Anterior uveitis
Eye Diseases 0.010 1.000 1 2011 2011
dbSNP: rs4505848
rs4505848
0.776 0.400 4 122211337 intron variant A/G snv 0.29
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.800 1.000 1 2009 2009
dbSNP: rs45510091
rs45510091
1.000 0.040 4 122265238 intron variant A/G snv 3.3E-02
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs45515895
rs45515895
4 122263672 intron variant G/A snv 0.16
Platelet mean volume determination (procedure)
0.700 1.000 1 2016 2016