Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11174202
rs11174202
0.925 0.040 12 61858476 intron variant A/G snv 0.49
CUI: C0003125
Disease: Anorexia Nervosa
Anorexia Nervosa
Mental Disorders 0.700 1.000 2 2017 2018
dbSNP: rs11174202
rs11174202
0.925 0.040 12 61858476 intron variant A/G snv 0.49
CUI: C0028768
Disease: Obsessive-Compulsive Disorder
Obsessive-Compulsive Disorder
Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs11174267
rs11174267
1.000 0.040 12 61992819 intron variant A/C;G snv 0.29
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
Respiratory Tract Diseases 0.700 1.000 1 2014 2014
dbSNP: rs11174267
rs11174267
1.000 0.040 12 61992819 intron variant A/C;G snv 0.29
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator
0.700 1.000 1 2015 2015
dbSNP: rs12815303
rs12815303
12 61993402 intron variant A/G snv 0.29
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator
0.700 1.000 1 2015 2015
dbSNP: rs12817007
rs12817007
12 61993501 intron variant T/C;G snv 0.29
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator
0.700 1.000 1 2015 2015
dbSNP: rs12817011
rs12817011
12 61993506 intron variant T/C snv 0.29
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator
0.700 1.000 1 2015 2015
dbSNP: rs17713040
rs17713040
12 62073933 intron variant T/C snv 1.6E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs1975494
rs1975494
1.000 0.040 12 62114416 intron variant A/G snv 0.22
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator
0.700 1.000 1 2015 2015
dbSNP: rs1975494
rs1975494
1.000 0.040 12 62114416 intron variant A/G snv 0.22
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
Respiratory Tract Diseases 0.700 1.000 1 2015 2015
dbSNP: rs2198776
rs2198776
12 61841052 intron variant C/T snv 0.33
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012
dbSNP: rs2198776
rs2198776
12 61841052 intron variant C/T snv 0.33
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2012 2012
dbSNP: rs3759289
rs3759289
12 61867674 intron variant C/G;T snv 0.81
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019