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: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.010 1.000 1 2018 2018
dbSNP: rs2069845
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.010 1.000 1 2018 2018
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0085693
Disease: Acute appendicitis NOS (disorder)
Acute appendicitis NOS (disorder)
0.010 1.000 1 2015 2015
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome
0.010 1.000 1 2012 2012
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome
0.010 1.000 1 2010 2010
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome
0.010 1.000 1 2010 2010
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: rs1800797
rs1800797
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C0856825
Disease: Acute GVH disease
Acute GVH disease
0.010 1.000 1 2015 2015
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis
0.010 < 0.001 1 2013 2013
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis
0.010 < 0.001 1 2013 2013
dbSNP: rs2066992
rs2066992
0.807 0.200 7 22728630 non coding transcript exon variant G/T snv 9.4E-02
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.010 1.000 1 2017 2017
dbSNP: rs2069840
rs2069840
0.742 0.360 7 22728953 intron variant C/G snv 0.27
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.010 1.000 1 2017 2017
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine
0.010 1.000 1 2010 2010
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
0.010 1.000 1 2010 2010
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C1332201
Disease: Adult Diffuse Large B-Cell Lymphoma
Adult Diffuse Large B-Cell Lymphoma
0.010 1.000 1 2015 2015
dbSNP: rs1800797
rs1800797
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C1332201
Disease: Adult Diffuse Large B-Cell Lymphoma
Adult Diffuse Large B-Cell Lymphoma
0.010 1.000 1 2018 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0220597
Disease: Adult Hodgkin Lymphoma
Adult Hodgkin Lymphoma
0.020 1.000 2 2013 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0220630
Disease: Adult Liver Carcinoma
Adult Liver Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs1800797
rs1800797
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C0220630
Disease: Adult Liver Carcinoma
Adult Liver Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs1800797
rs1800797
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C0741260
Disease: Adult onset asthma
Adult onset asthma
0.010 1.000 1 2016 2016
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0343640
Disease: African Burkitt's lymphoma
African Burkitt's lymphoma
0.010 1.000 1 2014 2014
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: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder)
0.010 1.000 1 2016 2016
dbSNP: rs1800797
rs1800797
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder)
0.010 1.000 1 2014 2014
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