Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs41423247
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31
CUI: C0011570
Disease: Mental Depression
Mental Depression 		0.030 1.000 3 2012 2018
dbSNP: rs41423247
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		0.030 1.000 3 2012 2018
dbSNP: rs41423247
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31
CUI: C0344315
Disease: Depressed mood
Depressed mood 		0.030 1.000 3 2012 2018
dbSNP: rs41423247
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31
CUI: C0013473
Disease: Eating Disorders
Eating Disorders 		0.030 1.000 3 2010 2016
dbSNP: rs41423247
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31
CUI: C4284586
Disease: Perinatal depression in mother
Perinatal depression in mother 		0.010 < 0.001 1 2015 2015
dbSNP: rs41423247
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31
CUI: C4552766
Disease: Miscarriage
Miscarriage 		0.010 1.000 1 2010 2010
dbSNP: rs41423247
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.010 < 0.001 1 2018 2018
dbSNP: rs41423247
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		0.010 1.000 1 2012 2012
dbSNP: rs41423247
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31
CUI: C0856825
Disease: Acute GVH disease
Acute GVH disease 		0.010 1.000 1 2015 2015
dbSNP: rs41423247
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.010 1.000 1 2016 2016
dbSNP: rs41423247
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31
CUI: C0600427
Disease: Cocaine Dependence
Cocaine Dependence 		0.010 1.000 1 2019 2019
dbSNP: rs41423247
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31
CUI: C0340100
Disease: High altitude pulmonary edema
High altitude pulmonary edema 		0.010 1.000 1 2019 2019
dbSNP: rs41423247
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31
CUI: C0004096
Disease: Asthma
Asthma 		0.010 1.000 1 2016 2016
dbSNP: rs41423247
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31
CUI: C0003125
Disease: Anorexia Nervosa
Anorexia Nervosa 		0.010 1.000 1 2016 2016
dbSNP: rs41423247
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31
CUI: C0233397
Disease: Psychological symptom
Psychological symptom 		0.010 1.000 1 2012 2012
dbSNP: rs41423247
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31
CUI: C0730314
Disease: Chronic central serous chorioretinopathy
Chronic central serous chorioretinopathy 		0.010 < 0.001 1 2017 2017
dbSNP: rs41423247
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression 		0.010 1.000 1 2016 2016
dbSNP: rs41423247
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.010 1.000 1 2020 2020
dbSNP: rs41423247
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms 		0.010 1.000 1 2016 2016
dbSNP: rs41423247
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31
CUI: C0010481
Disease: Cushing Syndrome
Cushing Syndrome 		0.010 1.000 1 2016 2016
dbSNP: rs41423247
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31
CUI: C0028754
Disease: Obesity
Obesity 		0.010 1.000 1 2010 2010
dbSNP: rs41423247
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31
CUI: C0342443
Disease: Adrenal Cushing's syndrome
Adrenal Cushing's syndrome 		0.010 1.000 1 2016 2016
dbSNP: rs41423247
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31
CUI: C0038436
Disease: Post-Traumatic Stress Disorder
Post-Traumatic Stress Disorder 		0.010 1.000 1 2018 2018