rs1979277, SHMT1

N. diseases: 45
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.
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1.000 1 2012 2012
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1.000 1 2007 2007
Adult Acute Lymphocytic Leukemia
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
154 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.030 1.000 3 2002 2012
Adult Non-Hodgkin Lymphoma
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
39 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1.000 1 2015 2015
Adult Solid Neoplasm
CUI: C0280099
Disease: Adult Solid Neoplasm
3 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1.000 1 2015 2015
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
395 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1.000 1 2009 2009
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.040 0.750 4 2010 2015
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.020 1.000 2 2007 2014
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.020 0.500 2 2005 2011
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.020 1.000 2 2012 2016
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1 2014 2014
Childhood Non-Hodgkin Lymphoma
CUI: C0220612
Disease: Childhood Non-Hodgkin Lymphoma
39 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1.000 1 2015 2015
Childhood Solid Neoplasm
CUI: C0279068
Disease: Childhood Solid Neoplasm
3 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1.000 1 2015 2015
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1.000 1 2010 2010
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.030 1.000 3 2013 2014
Complete Trisomy 21 Syndrome
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
77 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1.000 1 2012 2012
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.020 1.000 2 2013 2015
Down Syndrome
CUI: C0013080
Disease: Down Syndrome
80 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1.000 1 2012 2012
Extrapulmonary Small Cell Carcinoma
CUI: C4722419
Disease: Extrapulmonary Small Cell Carcinoma
11 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1.000 1 2007 2007
Gastric Cardia Adenocarcinoma
CUI: C1333762
Disease: Gastric Cardia Adenocarcinoma
11 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1.000 1 2007 2007
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1.000 1 2007 2007
Head and Neck Carcinoma
CUI: C3887461
Disease: Head and Neck Carcinoma
118 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1 2014 2014
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1.000 1 2018 2018
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1.000 1 2018 2018
Laryngeal Diseases
CUI: C0023051
Disease: Laryngeal Diseases
7 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1 2014 2014