rs1801198, TCN2

N. diseases: 26
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.020 1.000 2 2015 2017
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.020 1.000 2 2018 2019
Complete Trisomy 21 Syndrome
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
77 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.020 0.500 2 2008 2012
Down Syndrome
CUI: C0013080
Disease: Down Syndrome
80 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.020 0.500 2 2008 2012
Hyperhomocysteinemia
CUI: C0598608
Disease: Hyperhomocysteinemia
45 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.020 1.000 2 2003 2007
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.010 1.000 1 2007 2007
Anemia, Pernicious
CUI: C0002892
Disease: Anemia, Pernicious
4 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.010 1.000 1 2006 2006
ATRIAL SEPTAL DEFECT 1
CUI: C1862389
Disease: ATRIAL SEPTAL DEFECT 1
16 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.010 1.000 1 2019 2019
Atrial Septal Defects
CUI: C0018817
Disease: Atrial Septal Defects
96 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.010 1.000 1 2019 2019
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
263 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.010 1.000 1 2012 2012
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.010 1.000 1 2006 2006
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.010 1.000 1 2013 2013
Congenital Abnormality
CUI: C0000768
Disease: Congenital Abnormality
73 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.010 1.000 1 2017 2017
Congenital omphalocele
CUI: C0795690
Disease: Congenital omphalocele
13 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.010 1 2005 2005
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.010 1.000 1 2012 2012
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.010 1.000 1 2017 2017
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.010 1.000 1 2011 2011
Folic Acid Deficiency
CUI: C0016412
Disease: Folic Acid Deficiency
8 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.010 1.000 1 2017 2017
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.010 1.000 1 2006 2006
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.010 1.000 1 2006 2006
Neural Tube Defects
CUI: C0027794
Disease: Neural Tube Defects
122 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.010 1.000 1 2011 2011
Oral cleft
CUI: C4021813
Disease: Oral cleft
28 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.010 1.000 1 2020 2020
Peripheral Nervous System Diseases
CUI: C4721453
Disease: Peripheral Nervous System Diseases
69 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.010 1.000 1 2016 2016
Peripheral Neuropathy
CUI: C0031117
Disease: Peripheral Neuropathy
81 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.010 1.000 1 2016 2016
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.010 1.000 1 2017 2017