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: rs2069837
rs2069837
0.769 0.286 7 22728408 intron variant A/C,G snp 8.9E-02
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity
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: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.010 1.000 1 2013 2013
dbSNP: rs2069837
rs2069837
0.769 0.286 7 22728408 intron variant A/C,G snp 8.9E-02
CUI: C0039263
Disease: Takayasu Arteritis
Takayasu Arteritis
0.010 1.000 1 2015 2015
dbSNP: rs2069837
rs2069837
0.769 0.286 7 22728408 intron variant A/C,G snp 8.9E-02
CUI: C0023980
Disease: Longevity
Longevity
0.700 1 2016 2016
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: rs2069837
rs2069837
0.769 0.286 7 22728408 intron variant A/C,G snp 8.9E-02
CUI: C0023529
Disease: Leukomalacia, Periventricular
Leukomalacia, Periventricular
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: C4048328
Disease: cervical cancer
cervical cancer
0.010 1.000 1 2013 2013
dbSNP: rs2069837
rs2069837
0.769 0.286 7 22728408 intron variant A/C,G snp 8.9E-02
CUI: C0426970
Disease: Spastic Quadriplegia
Spastic Quadriplegia
0.010 1.000 1 2013 2013
dbSNP: rs2069837
rs2069837
0.769 0.286 7 22728408 intron variant A/C,G snp 8.9E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 1.000 1 2012 2012
dbSNP: rs2069837
rs2069837
0.769 0.286 7 22728408 intron variant A/C,G snp 8.9E-02
CUI: C0443306
Disease: Spastic
Spastic
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: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs1800797
rs1800797
0.692 0.464 7 22726602 non coding transcript exon variant A/G snp 0.69
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis
0.020 1.000 2 2008 2010
dbSNP: rs1800797
rs1800797
0.692 0.464 7 22726602 non coding transcript exon variant A/G snp 0.69
Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
0.010 1.000 1 2016 2016
dbSNP: rs1800797
rs1800797
0.692 0.464 7 22726602 non coding transcript exon variant A/G snp 0.69
CUI: C0023343
Disease: Leprosy
Leprosy
0.010 1.000 1 2011 2011
dbSNP: rs1800797
rs1800797
0.692 0.464 7 22726602 non coding transcript exon variant A/G snp 0.69
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.010 1.000 1 2010 2010
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: rs1800797
rs1800797
0.692 0.464 7 22726602 non coding transcript exon variant A/G snp 0.69
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 1.000 1 2017 2017
dbSNP: rs1800797
rs1800797
0.692 0.464 7 22726602 non coding transcript exon variant A/G snp 0.69
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs1800797
rs1800797
0.692 0.464 7 22726602 non coding transcript exon variant A/G snp 0.69
CUI: C0028754
Disease: Obesity
Obesity
0.010 1.000 1 2010 2010
dbSNP: rs1800797
rs1800797
0.692 0.464 7 22726602 non coding transcript exon variant A/G snp 0.69
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2017 2017
dbSNP: rs1800797
rs1800797
0.692 0.464 7 22726602 non coding transcript exon variant A/G snp 0.69
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.010 1.000 1 2009 2009
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: rs1800797
rs1800797
0.692 0.464 7 22726602 non coding transcript exon variant A/G snp 0.69
CUI: C0011206
Disease: Delirium
Delirium
0.010 < 0.001 1 2011 2011
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
dbSNP: rs1800797
rs1800797
0.692 0.464 7 22726602 non coding transcript exon variant A/G snp 0.69
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.010 1.000 1 2009 2009