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: rs2069705
rs2069705
0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.020 0.500 2 2012 2012
dbSNP: rs2069705
rs2069705
0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.020 0.500 2 2012 2012
dbSNP: rs2069705
rs2069705
0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.020 1.000 2 2010 2016
dbSNP: rs2069705
rs2069705
0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary
0.010 1.000 1 2017 2017
dbSNP: rs2069705
rs2069705
0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0030193
Disease: Pain
Pain
0.010 1.000 1 2017 2017
dbSNP: rs2069705
rs2069705
0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.010 1.000 1 2019 2019
dbSNP: rs2069705
rs2069705
0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0023281
Disease: Leishmaniasis
Leishmaniasis
0.010 1.000 1 2019 2019
dbSNP: rs2069705
rs2069705
0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0024530
Disease: Malaria
Malaria
0.010 1.000 1 2014 2014
dbSNP: rs2069705
rs2069705
0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.010 1.000 1 2020 2020
dbSNP: rs2069705
rs2069705
0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs2069705
rs2069705
0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0002893
Disease: Refractory anemias
Refractory anemias
0.010 1.000 1 2020 2020
dbSNP: rs2069705
rs2069705
0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0023283
Disease: Leishmaniasis, Cutaneous
Leishmaniasis, Cutaneous
0.010 1.000 1 2019 2019
dbSNP: rs2069705
rs2069705
0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0333307
Disease: Superficial ulcer
Superficial ulcer
0.010 1.000 1 2020 2020
dbSNP: rs2069705
rs2069705
0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0004096
Disease: Asthma
Asthma
0.010 1.000 1 2008 2008
dbSNP: rs2069705
rs2069705
0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0085568
Disease: Buruli Ulcer
Buruli Ulcer
0.010 1.000 1 2017 2017
dbSNP: rs2069705
rs2069705
0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome
0.010 1.000 1 2019 2019
dbSNP: rs2069705
rs2069705
0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0015967
Disease: Fever
Fever
0.010 1.000 1 2012 2012
dbSNP: rs2069705
rs2069705
0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0026272
Disease: Mixed Connective Tissue Disease
Mixed Connective Tissue Disease
0.010 1.000 1 2019 2019
dbSNP: rs2069705
rs2069705
0.695 0.440 12 68161231 intron variant G/A;C snv
CUI: C0014060
Disease: Encephalitis, St. Louis
Encephalitis, St. Louis
0.010 1.000 1 2010 2010
dbSNP: rs2069707
rs2069707
0.925 0.120 12 68160508 intron variant G/A;C snv
CUI: C0031049
Disease: Pericarditis, Tuberculous
Pericarditis, Tuberculous
0.010 1.000 1 2018 2018
dbSNP: rs2069707
rs2069707
0.925 0.120 12 68160508 intron variant G/A;C snv
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.010 1.000 1 2015 2015
dbSNP: rs2069727
rs2069727
0.763 0.320 12 68154443 intron variant T/A;C snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.010 1.000 1 2010 2010
dbSNP: rs2069727
rs2069727
0.763 0.320 12 68154443 intron variant T/A;C snv
CUI: C0856825
Disease: Acute GVH disease
Acute GVH disease
0.010 1.000 1 2015 2015
dbSNP: rs2069727
rs2069727
0.763 0.320 12 68154443 intron variant T/A;C snv
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome
0.010 1.000 1 2019 2019
dbSNP: rs2069727
rs2069727
0.763 0.320 12 68154443 intron variant T/A;C snv
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia
0.010 1.000 1 2010 2010