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: rs11030104
rs11030104
0.790 0.240 11 27662970 intron variant A/G snv 0.16
CUI: C0281899
Disease: Prolapsed lumbar disc
Prolapsed lumbar disc
0.010 1.000 1 2018 2018
dbSNP: rs11030104
rs11030104
0.790 0.240 11 27662970 intron variant A/G snv 0.16
CUI: C0030319
Disease: Panic Disorder
Panic Disorder
0.010 1.000 1 2009 2009
dbSNP: rs11030104
rs11030104
0.790 0.240 11 27662970 intron variant A/G snv 0.16
CUI: C0344315
Disease: Depressed mood
Depressed mood
0.010 1.000 1 2015 2015
dbSNP: rs11030107
rs11030107
1.000 0.040 11 27673288 intron variant A/G snv 0.19
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders
0.010 1.000 1 2018 2018
dbSNP: rs11030107
rs11030107
1.000 0.040 11 27673288 intron variant A/G snv 0.19
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.010 1.000 1 2012 2012
dbSNP: rs11030108
rs11030108
1.000 0.040 11 27673917 intron variant A/G snv 0.72
CUI: C0234985
Disease: Mental deterioration
Mental deterioration
0.010 1.000 1 2013 2013
dbSNP: rs11030108
rs11030108
1.000 0.040 11 27673917 intron variant A/G snv 0.72
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
0.010 1.000 1 2013 2013
dbSNP: rs12273539
rs12273539
0.925 0.120 11 27661764 intron variant C/T snv 0.12
CUI: C0016053
Disease: Fibromyalgia
Fibromyalgia
0.010 1.000 1 2018 2018
dbSNP: rs12273539
rs12273539
0.925 0.120 11 27661764 intron variant C/T snv 0.12
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.010 1.000 1 2009 2009
dbSNP: rs12291063
rs12291063
1.000 0.080 11 27672554 intron variant T/C snv 0.12
CUI: C0028754
Disease: Obesity
Obesity
0.010 1.000 1 2015 2015
dbSNP: rs1243188371
rs1243188371
1.000 0.160 11 27674117 synonymous variant C/T snv 4.1E-06 7.0E-06
CUI: C0019202
Disease: Hepatolenticular Degeneration
Hepatolenticular Degeneration
0.010 1.000 1 2013 2013
dbSNP: rs1339220115
rs1339220115
1.000 0.080 11 27658119 missense variant G/A snv 4.0E-06 7.0E-06
CUI: C0035372
Disease: Rett Syndrome
Rett Syndrome
0.010 1.000 1 2009 2009
dbSNP: rs1349681470
rs1349681470
1.000 0.080 11 27658333 missense variant G/A snv 1.4E-05
CUI: C0035372
Disease: Rett Syndrome
Rett Syndrome
0.010 1.000 1 2009 2009
dbSNP: rs1401635
rs1401635
0.925 0.040 11 27672444 intron variant C/G snv 0.73
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression
0.010 1.000 1 2015 2015
dbSNP: rs1401635
rs1401635
0.925 0.040 11 27672444 intron variant C/G snv 0.73
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.010 1.000 1 2015 2015
dbSNP: rs1415125856
rs1415125856
0.827 0.120 11 27658550 splice region variant G/A snv 4.0E-06 2.1E-05
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.010 1.000 1 2013 2013
dbSNP: rs1415125856
rs1415125856
0.827 0.120 11 27658550 splice region variant G/A snv 4.0E-06 2.1E-05
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.010 1.000 1 2013 2013
dbSNP: rs1415125856
rs1415125856
0.827 0.120 11 27658550 splice region variant G/A snv 4.0E-06 2.1E-05
CUI: C0344315
Disease: Depressed mood
Depressed mood
0.010 1.000 1 2013 2013
dbSNP: rs1415125856
rs1415125856
0.827 0.120 11 27658550 splice region variant G/A snv 4.0E-06 2.1E-05
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.010 1.000 1 2019 2019
dbSNP: rs1415125856
rs1415125856
0.827 0.120 11 27658550 splice region variant G/A snv 4.0E-06 2.1E-05
CUI: C0549622
Disease: Sexual Dysfunction
Sexual Dysfunction
0.010 1.000 1 2019 2019
dbSNP: rs1415125856
rs1415125856
0.827 0.120 11 27658550 splice region variant G/A snv 4.0E-06 2.1E-05
CUI: C2938940
Disease: Post stroke depression
Post stroke depression
0.010 1.000 1 2016 2016
dbSNP: rs1415125856
rs1415125856
0.827 0.120 11 27658550 splice region variant G/A snv 4.0E-06 2.1E-05
CUI: C0011570
Disease: Mental Depression
Mental Depression
0.010 1.000 1 2013 2013
dbSNP: rs1431475678
rs1431475678
1.000 0.120 11 27658555 missense variant G/C snv 7.0E-06
CUI: C0751072
Disease: Frontotemporal Lobar Degeneration
Frontotemporal Lobar Degeneration
0.010 1.000 1 2012 2012
dbSNP: rs1451603364
rs1451603364
0.925 0.120 11 27658411 missense variant C/T snv 4.0E-06
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder
0.010 1.000 1 2016 2016
dbSNP: rs1451603364
rs1451603364
0.925 0.120 11 27658411 missense variant C/T snv 4.0E-06
Diabetes Mellitus, Non-Insulin-Dependent
0.010 1.000 1 2016 2016