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: 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: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine
0.010 1.000 1 2010 2010
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: 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: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.010 1.000 1 2014 2014
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: C0004610
Disease: Bacteremia
Bacteremia
0.010 1.000 1 2016 2016
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: rs1800796
rs1800796
0.647 0.571 7 22726627 non coding transcript exon variant G/C snp 0.10
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2007 2007
dbSNP: rs1800797
rs1800797
0.692 0.464 7 22726602 non coding transcript exon variant A/G snp 0.69
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2007 2007
dbSNP: rs2069832
rs2069832
0.878 0.107 7 22727814 intron variant A/G,T snp 0.68
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2008 2008
dbSNP: rs2069861
rs2069861
IL6
0.923 0.071 7 22732035 intergenic variant C/A,T snp 5.9E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 < 0.001 1 2012 2012
dbSNP: rs1800796
rs1800796
0.647 0.571 7 22726627 non coding transcript exon variant G/C snp 0.10
CUI: C0006625
Disease: Cachexia
Cachexia
0.010 1.000 1 2015 2015
dbSNP: rs1800796
rs1800796
0.647 0.571 7 22726627 non coding transcript exon variant G/C snp 0.10
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 1.000 1 2014 2014
dbSNP: rs1800797
rs1800797
0.692 0.464 7 22726602 non coding transcript exon variant A/G snp 0.69
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 1.000 1 2017 2017
dbSNP: rs2069825
rs2069825
1.000 0.036 7 22725718 non coding transcript exon variant T/TCC in-del 2.4E-04
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.010 1.000 1 2011 2011
dbSNP: rs2069840
rs2069840
0.923 0.071 7 22728953 intron variant C/G snp 0.26
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular 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: 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: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2011 2011
dbSNP: rs1800796
rs1800796
0.647 0.571 7 22726627 non coding transcript exon variant G/C snp 0.10
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2014 2014
dbSNP: rs2066992
rs2066992
1.000 0.036 7 22728630 non coding transcript exon variant G/T snp 9.8E-02
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2014 2014
dbSNP: rs2069837
rs2069837
0.769 0.286 7 22728408 intron variant A/C,G snp 8.9E-02
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2014 2014
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.010 1.000 1 2016 2016
dbSNP: rs1800795
rs1800795
0.580 0.607 7 22727026 intron variant C/G snp 0.68
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.010 1.000 1 2018 2018
dbSNP: rs1800797
rs1800797
0.692 0.464 7 22726602 non coding transcript exon variant A/G snp 0.69
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.010 1.000 1 2009 2009