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.
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
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
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1.000 1 2007 2007
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
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
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
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
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
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
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
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
348 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 1.000 1 2012 2012
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.020 1.000 2 2010 2013
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.020 1.000 2 2010 2013
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
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
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
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
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
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
CUI: C4722085
Disease: 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