Source: BEFREE

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: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.900 0.944 29 2006 2020
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.900 0.773 19 2006 2020
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.900 1.000 12 2007 2020
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.900 0.857 12 2008 2018
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.900 1.000 11 2008 2018
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.070 0.714 7 2009 2020
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic
0.040 1.000 4 2008 2019
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0004096
Disease: Asthma
Asthma
0.020 1.000 2 2015 2016
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.020 1.000 2 2011 2011
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome
0.010 1.000 1 2009 2009
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0271907
Disease: Acquired aplastic anemia
Acquired aplastic anemia
0.010 < 0.001 1 2009 2009
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0151281
Disease: Genital ulcers
Genital ulcers
0.010 1.000 1 2014 2014
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.010 1.000 1 2015 2015
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 < 0.001 1 2015 2015
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 < 0.001 1 2015 2015
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.010 1.000 1 2008 2008
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0031099
Disease: Periodontitis
Periodontitis
0.010 1.000 1 2013 2013
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0151517
Disease: Complete atrioventricular block
Complete atrioventricular block
0.010 1.000 1 2017 2017
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0339143
Disease: Thyroid associated opthalmopathies
Thyroid associated opthalmopathies
0.010 < 0.001 1 2008 2008
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0574960
Disease: Sacroiliitis
Sacroiliitis
0.010 1.000 1 2013 2013
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C2931133
Disease: Pediatric Crohn's disease
Pediatric Crohn's disease
0.010 1.000 1 2007 2007
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0949690
Disease: Spondylarthritis
Spondylarthritis
0.010 1.000 1 2013 2013
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.010 < 0.001 1 2008 2008
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
Diabetes Mellitus, Insulin-Dependent
0.010 < 0.001 1 2013 2013