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: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
CUI: C0008707
Disease: Chronic osteomyelitis
Chronic osteomyelitis
0.700 0
dbSNP: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.800 1.000 1 2011 2011
dbSNP: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.800 1.000 1 2010 2010
dbSNP: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
0.800 1.000 1 2014 2014
dbSNP: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2010 2010
dbSNP: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.700 1.000 1 2010 2010
dbSNP: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma
0.700 1.000 1 2014 2014
dbSNP: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 1 2010 2010
dbSNP: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
Malignant neoplasm of large intestine
0.700 1.000 1 2010 2010
dbSNP: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2010 2010
dbSNP: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2010 2010
dbSNP: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.700 1.000 1 2010 2010
dbSNP: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial
0.700 1.000 1 2013 2013
dbSNP: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 1 2010 2010
dbSNP: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 1.000 1 2017 2017
dbSNP: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.010 1.000 1 2017 2017
dbSNP: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
CUI: C0278877
Disease: Adult Meningioma
Adult Meningioma
0.010 1.000 1 2019 2019
dbSNP: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 1.000 1 2017 2017
dbSNP: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
Meningioma, benign, no ICD-O subtype
0.010 1.000 1 2019 2019
dbSNP: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine
0.010 1.000 1 2012 2012
dbSNP: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
ANOPHTHALMIA AND PULMONARY HYPOPLASIA
0.010 1.000 1 2019 2019
dbSNP: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2017 2017
dbSNP: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.010 1.000 1 2017 2017
dbSNP: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
CUI: C0025286
Disease: Meningioma
Meningioma
0.010 1.000 1 2019 2019
dbSNP: rs10936599
rs10936599
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.010 1.000 1 2019 2019