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
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.040 1.000 4 2007 2013
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.040 1.000 4 2007 2013
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.030 1.000 3 2013 2015
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.720 1.000 3 2012 2016
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.030 1.000 3 2013 2015
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.030 0.667 3 2009 2018
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
Diabetes Mellitus, Non-Insulin-Dependent
0.030 1.000 3 2006 2012
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.030 0.667 3 2009 2018
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms
0.020 1.000 2 2010 2016
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.020 1.000 2 2011 2016
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C1527249
Disease: Colorectal Cancer
Colorectal Cancer
0.020 1.000 2 2008 2017
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.020 1.000 2 2012 2016
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma
0.020 1.000 2 2009 2014
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0015672
Disease: Fatigue
Fatigue
0.020 1.000 2 2012 2013
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
Diabetes Mellitus, Insulin-Dependent
0.020 1.000 2 2009 2016
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis
0.020 1.000 2 2008 2010
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma
0.020 1.000 2 2009 2014
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.020 1.000 2 2008 2017
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.020 1.000 2 2009 2012
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.010 1.000 1 2006 2006
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
0.010 1.000 1 2017 2017
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0856825
Disease: Acute GVH disease
Acute GVH disease
0.010 1.000 1 2012 2012
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.010 1.000 1 2009 2009
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
0.010 1.000 1 2014 2014
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.010 1.000 1 2018 2018