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: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.720 1.000 3 2012 2016
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
Diabetes Mellitus, Non-Insulin-Dependent
0.070 1.000 7 2006 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.070 0.714 7 2009 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.070 0.714 7 2009 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.060 1.000 6 2007 2017
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.060 0.833 6 2010 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.060 1.000 6 2007 2017
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.050 1.000 5 2009 2017
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.040 1.000 4 2018 2020
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.040 1.000 4 2017 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.040 1.000 4 2017 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.040 1.000 4 2017 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.040 0.750 4 2007 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.040 1.000 4 2014 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.040 0.750 4 2007 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.030 1.000 3 2011 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma
0.030 1.000 3 2009 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis
0.030 1.000 3 2008 2014
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.030 1.000 3 2012 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms
0.030 1.000 3 2010 2016
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C4086165
Disease: Childhood Neuroblastoma
Childhood Neuroblastoma
0.030 1.000 3 2009 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.030 1.000 3 2007 2016
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma
0.030 1.000 3 2009 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0022104
Disease: Irritable Bowel Syndrome
Irritable Bowel Syndrome
0.020 1.000 2 2017 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.020 1.000 2 2012 2014