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 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
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
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
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
Laryngeal neoplasm
CUI: C0023055
Disease: Laryngeal neoplasm
1 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1.000 1 2014 2014
leukemia
CUI: C0023418
Disease: leukemia
144 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1 2014 2014
Lymphoma, Non-Hodgkin, Familial
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
79 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1.000 1 2015 2015
Malignant Head and Neck Neoplasm
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
118 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1 2014 2014
Malignant neoplasm of colon and/or rectum
502 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1.000 1 2014 2014
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1.000 1 2010 2010
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1 2019 2019