FKBP5, FKBP prolyl isomerase 5, 2289

N. diseases: 179; N. variants: 20
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs16878812
rs16878812 		0.776 0.080 6 35601785 intron variant A/G snv 0.15
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 2 2019 2019
dbSNP: rs16878812
rs16878812 		0.776 0.080 6 35601785 intron variant A/G snv 0.15
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		Digestive System Diseases; Neoplasms 0.700 1.000 2 2019 2019
dbSNP: rs16878812
rs16878812 		0.776 0.080 6 35601785 intron variant A/G snv 0.15
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 2 2019 2019
dbSNP: rs16878812
rs16878812 		0.776 0.080 6 35601785 intron variant A/G snv 0.15
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		Digestive System Diseases; Neoplasms 0.700 1.000 2 2019 2019
dbSNP: rs16878812
rs16878812 		0.776 0.080 6 35601785 intron variant A/G snv 0.15
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 2 2019 2019
dbSNP: rs16878812
rs16878812 		0.776 0.080 6 35601785 intron variant A/G snv 0.15
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 2 2019 2019
dbSNP: rs16878812
rs16878812 		0.776 0.080 6 35601785 intron variant A/G snv 0.15
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 1.000 2 2019 2019
dbSNP: rs16878812
rs16878812 		0.776 0.080 6 35601785 intron variant A/G snv 0.15
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 2 2019 2019
dbSNP: rs16878812
rs16878812 		0.776 0.080 6 35601785 intron variant A/G snv 0.15
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 2 2019 2019
dbSNP: rs12200498
rs12200498 		6 35718178 intron variant G/A snv 0.14
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1334894
rs1334894 		1.000 0.040 6 35647353 intron variant C/T snv 6.6E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs140664762
rs140664762 		6 35586294 3 prime UTR variant G/A snv 5.3E-03
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs16878812
rs16878812 		0.776 0.080 6 35601785 intron variant A/G snv 0.15
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs28435135
rs28435135 		6 35727814 intron variant C/G;T snv
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs3798345
rs3798345 		6 35594694 intron variant T/A;C snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs7740395
rs7740395 		6 35635195 intron variant C/G;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs9348981
rs9348981 		6 35719472 intron variant T/G snv 0.27
CUI: C0005612
Disease: Birth Weight
Birth Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2019 2019
dbSNP: rs1360780
rs1360780 		0.708 0.320 6 35639794 intron variant T/A;C snv
CUI: C4016801
Disease: MAJOR DEPRESSIVE DISORDER, INCREASED RECURRENCE OF DEPRESSIVE EPISODES IN, SUSCEPTIBILITY TO
MAJOR DEPRESSIVE DISORDER, INCREASED RECURRENCE OF DEPRESSIVE EPISODES IN, SUSCEPTIBILITY TO 		0.700 0
dbSNP: rs1360780
rs1360780 		0.708 0.320 6 35639794 intron variant T/A;C snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.090 1.000 9 2010 2019
dbSNP: rs1360780
rs1360780 		0.708 0.320 6 35639794 intron variant T/A;C snv
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		Mental Disorders 0.090 1.000 9 2010 2019
dbSNP: rs1360780
rs1360780 		0.708 0.320 6 35639794 intron variant T/A;C snv
CUI: C0344315
Disease: Depressed mood
Depressed mood 		Behavior and Behavior Mechanisms 0.080 1.000 8 2010 2019
dbSNP: rs1360780
rs1360780 		0.708 0.320 6 35639794 intron variant T/A;C snv
CUI: C0011570
Disease: Mental Depression
Mental Depression 		Behavior and Behavior Mechanisms 0.080 1.000 8 2010 2019
dbSNP: rs1360780
rs1360780 		0.708 0.320 6 35639794 intron variant T/A;C snv
CUI: C0038436
Disease: Post-Traumatic Stress Disorder
Post-Traumatic Stress Disorder 		Mental Disorders 0.060 1.000 6 2013 2019
dbSNP: rs9470080
rs9470080 		0.827 0.080 6 35678658 intron variant T/A;C snv
CUI: C0038436
Disease: Post-Traumatic Stress Disorder
Post-Traumatic Stress Disorder 		Mental Disorders 0.060 0.833 6 2008 2019
dbSNP: rs9296158
rs9296158 		0.763 0.080 6 35599305 intron variant A/G snv 0.65
CUI: C0038436
Disease: Post-Traumatic Stress Disorder
Post-Traumatic Stress Disorder 		Mental Disorders 0.050 0.800 5 2008 2019