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: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.080 0.875 8 2005 2018
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C0014544
Disease: Epilepsy
Epilepsy
0.080 0.875 8 2007 2018
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.080 0.875 8 2005 2017
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.070 1.000 7 2008 2013
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C0027947
Disease: Neutropenia
Neutropenia
0.050 1.000 5 2007 2017
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C0023530
Disease: Leukopenia
Leukopenia
0.050 1.000 5 2007 2017
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.040 0.750 4 2010 2019
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
Malignant neoplasm of colon and/or rectum
0.040 1.000 4 2008 2013
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C1096063
Disease: Drug Resistant Epilepsy
Drug Resistant Epilepsy
0.040 1.000 4 2008 2017
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
Diffuse Large B-Cell Lymphoma
0.040 1.000 4 2013 2016
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.040 1.000 4 2002 2019
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
Myeloid Leukemia, Chronic
0.040 0.750 4 2014 2017
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.040 1.000 4 2006 2013
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.030 0.333 3 2007 2019
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C1704321
Disease: Nephrotic Syndrome, Minimal Change
Nephrotic Syndrome, Minimal Change
0.030 1.000 3 2015 2017
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C3496337
Disease: Idiopathic Nephrotic Syndrome
Idiopathic Nephrotic Syndrome
0.030 1.000 3 2015 2017
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial
0.030 1.000 3 2006 2013
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C1533172
Disease: Infantile nystagmus syndrome
Infantile nystagmus syndrome
0.030 0.667 3 2015 2017
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia
0.030 1.000 3 2008 2019
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C0392156
Disease: Akathisia
Akathisia
0.020 1.000 2 2010 2017
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression
0.020 < 0.001 2 2007 2008
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.020 1.000 2 2002 2011
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C0030193
Disease: Pain
Pain
0.020 1.000 2 2010 2017
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.020 1.000 2 2014 2016
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.020 1.000 2 2004 2015