Source: BEFREE

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: rs988712
rs988712
0.925 0.160 11 27541835 intron variant G/A;T snv
CUI: C0028754
Disease: Obesity
Obesity
0.810 1.000 1 2011 2018
dbSNP: rs1048218
rs1048218
1.000 0.080 11 27658340 missense variant C/A snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.010 1.000 1 2008 2008
dbSNP: rs1048220
rs1048220
1.000 0.040 11 27658191 missense variant C/A snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.010 1.000 1 2019 2019
dbSNP: rs10835210
rs10835210
0.882 0.040 11 27674363 intron variant C/A;G snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.010 1.000 1 2012 2012
dbSNP: rs10835210
rs10835210
0.882 0.040 11 27674363 intron variant C/A;G snv
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders
0.010 1.000 1 2018 2018
dbSNP: rs10835210
rs10835210
0.882 0.040 11 27674363 intron variant C/A;G snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.010 1.000 1 2009 2009
dbSNP: rs10835211
rs10835211
1.000 0.080 11 27679818 intron variant G/A snv 0.19
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders
0.010 1.000 1 2015 2015
dbSNP: rs11030064
rs11030064
1.000 0.080 11 27596469 intron variant C/T snv 0.41
CUI: C0281899
Disease: Prolapsed lumbar disc
Prolapsed lumbar disc
0.010 1.000 1 2018 2018
dbSNP: rs11030096
rs11030096
0.925 0.160 11 27643996 intron variant T/A;C snv
CUI: C0281899
Disease: Prolapsed lumbar disc
Prolapsed lumbar disc
0.010 1.000 1 2018 2018
dbSNP: rs11030096
rs11030096
0.925 0.160 11 27643996 intron variant T/A;C snv
CUI: C0085281
Disease: Addictive Behavior
Addictive Behavior
0.010 1.000 1 2016 2016
dbSNP: rs11030096
rs11030096
0.925 0.160 11 27643996 intron variant T/A;C snv
CUI: C0019337
Disease: Heroin Dependence
Heroin Dependence
0.010 1.000 1 2016 2016
dbSNP: rs11030100
rs11030100
1.000 0.080 11 27656039 3 prime UTR variant G/T snv 0.17
CUI: C0004096
Disease: Asthma
Asthma
0.010 1.000 1 2009 2009
dbSNP: rs11030101
rs11030101
0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36
CUI: C0004096
Disease: Asthma
Asthma
0.010 1.000 1 2009 2009
dbSNP: rs11030101
rs11030101
0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36
CUI: C0871388
Disease: social stress
social stress
0.010 1.000 1 2014 2014
dbSNP: rs11030101
rs11030101
0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.010 1.000 1 2012 2012
dbSNP: rs11030101
rs11030101
0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36
CUI: C0011570
Disease: Mental Depression
Mental Depression
0.010 1.000 1 2013 2013
dbSNP: rs11030101
rs11030101
0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36
CUI: C0344315
Disease: Depressed mood
Depressed mood
0.010 1.000 1 2013 2013
dbSNP: rs11030101
rs11030101
0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36
Depressive Disorder, Treatment-Resistant
0.010 1.000 1 2013 2013
dbSNP: rs11030101
rs11030101
0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.010 1.000 1 2012 2012
dbSNP: rs11030101
rs11030101
0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.010 1.000 1 2013 2013
dbSNP: rs11030104
rs11030104
0.790 0.240 11 27662970 intron variant A/G snv 0.16
CUI: C0019337
Disease: Heroin Dependence
Heroin Dependence
0.010 1.000 1 2016 2016
dbSNP: rs11030104
rs11030104
0.790 0.240 11 27662970 intron variant A/G snv 0.16
CUI: C0011570
Disease: Mental Depression
Mental Depression
0.010 1.000 1 2015 2015
dbSNP: rs11030104
rs11030104
0.790 0.240 11 27662970 intron variant A/G snv 0.16
CUI: C0016053
Disease: Fibromyalgia
Fibromyalgia
0.010 1.000 1 2018 2018
dbSNP: rs11030104
rs11030104
0.790 0.240 11 27662970 intron variant A/G snv 0.16
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.010 1.000 1 2015 2015
dbSNP: rs11030104
rs11030104
0.790 0.240 11 27662970 intron variant A/G snv 0.16
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.010 1.000 1 2015 2015