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: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
0.020 1.000 2 2015 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.020 1.000 2 2011 2013
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0856825
Disease: Acute GVH disease
Acute GVH disease
0.020 1.000 2 2012 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.020 1.000 2 2012 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.020 1.000 2 2012 2014
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0028754
Disease: Obesity
Obesity
0.020 0.500 2 2017 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.020 0.500 2 2014 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
Diabetes Mellitus, Insulin-Dependent
0.020 1.000 2 2009 2015
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.020 0.500 2 2018 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
0.020 1.000 2 2016 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder)
0.020 1.000 2 2014 2016
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.020 1.000 2 2017 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0595995
Disease: Idiopathic scoliosis
Idiopathic scoliosis
0.020 1.000 2 2015 2016
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.020 1.000 2 2014 2015
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0243026
Disease: Sepsis
Sepsis
0.010 1.000 1 2015 2015
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.010 1.000 1 2015 2015
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0042166
Disease: Uveitis, Intermediate
Uveitis, Intermediate
0.010 1.000 1 2015 2015
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0520679
Disease: Sleep Apnea, Obstructive
Sleep Apnea, Obstructive
0.010 1.000 1 2018 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.010 1.000 1 2017 2017
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.010 1.000 1 2012 2012
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C1719672
Disease: Severe Sepsis
Severe Sepsis
0.010 1.000 1 2015 2015
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2007 2007
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
Necrotizing enterocolitis in fetus OR newborn
0.010 1.000 1 2015 2015
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.010 1.000 1 2014 2014
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0014544
Disease: Epilepsy
Epilepsy
0.010 < 0.001 1 2012 2012