rs737865, TXNRD2;COMT

N. diseases: 11
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.
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.763 0.240 22 19942598 intron variant A/G snv 0.23 0.090 0.889 9 2004 2017
Anencephaly
CUI: C0002902
Disease: Anencephaly
10 0.763 0.240 22 19942598 intron variant A/G snv 0.23 0.020 1.000 2 2014 2015
Neural Tube Defects
CUI: C0027794
Disease: Neural Tube Defects
122 0.763 0.240 22 19942598 intron variant A/G snv 0.23 0.020 1.000 2 2014 2015
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.763 0.240 22 19942598 intron variant A/G snv 0.23 0.010 1.000 1 2008 2008
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
1451 0.763 0.240 22 19942598 intron variant A/G snv 0.23 0.010 1.000 1 2011 2011
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.763 0.240 22 19942598 intron variant A/G snv 0.23 0.010 1.000 1 2008 2008
NEUROTICISM
CUI: C1842981
Disease: NEUROTICISM
54 0.763 0.240 22 19942598 intron variant A/G snv 0.23 0.010 1.000 1 2005 2005
Nonorganic psychosis
CUI: C0349204
Disease: Nonorganic psychosis
98 0.763 0.240 22 19942598 intron variant A/G snv 0.23 0.010 1.000 1 2007 2007
Psychotic Disorders
CUI: C0033975
Disease: Psychotic Disorders
179 0.763 0.240 22 19942598 intron variant A/G snv 0.23 0.010 1.000 1 2007 2007
Spina Bifida
CUI: C0080178
Disease: Spina Bifida
61 0.763 0.240 22 19942598 intron variant A/G snv 0.23 0.010 1.000 1 2011 2011
Unipolar Depression
CUI: C0041696
Disease: Unipolar Depression
225 0.763 0.240 22 19942598 intron variant A/G snv 0.23 0.010 1.000 1 2011 2011