Source: GWASCAT

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: rs2910032
rs2910032
1.000 0.040 5 153160794 intron variant C/T snv 0.52
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.800 1.000 5 2013 2019
dbSNP: rs111294930
rs111294930
1.000 0.040 5 152797561 intron variant A/G snv 0.20
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 3 2014 2018
dbSNP: rs113568682
rs113568682
1.000 0.040 5 152920194 intron variant A/T snv 0.21
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 2 2017 2019
dbSNP: rs10070616
rs10070616
5 153174146 intron variant C/T snv 0.33
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms
0.700 1.000 1 2016 2016
dbSNP: rs1036605
rs1036605
1.000 0.040 5 153116973 intron variant A/G snv 0.33
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs113897692
rs113897692
1.000 0.040 5 152797226 intron variant A/G snv 0.20
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 1 2019 2019
dbSNP: rs12153740
rs12153740
1.000 0.040 5 152697204 intron variant T/A;C snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 1.000 1 2019 2019
dbSNP: rs1371063
rs1371063
1.000 0.040 5 153119610 intron variant T/C snv 0.49
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs1422560
rs1422560
5 153170644 intron variant T/A;G snv
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 1.000 1 2018 2018
dbSNP: rs17113985
rs17113985
1.000 0.040 5 153087229 intron variant G/A snv 2.5E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs17493476
rs17493476
1.000 0.040 5 153103246 intron variant T/G snv 0.14
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs17494099
rs17494099
1.000 0.040 5 153120463 intron variant A/G snv 0.11
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs17578068
rs17578068
1.000 0.040 5 153109462 intron variant T/A snv 0.11
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs17578145
rs17578145
1.000 0.040 5 153111905 intron variant A/C;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs2043847
rs2043847
1.000 0.040 5 153120252 intron variant G/C snv 0.53
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs2579040
rs2579040
5 153136263 intron variant T/A snv 0.72
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs2910032
rs2910032
1.000 0.040 5 153160794 intron variant C/T snv 0.52
Child Development Disorders, Pervasive
0.700 1.000 1 2017 2017
dbSNP: rs4958568
rs4958568
5 152636533 intron variant G/A snv 0.25
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs4958608
rs4958608
1.000 0.040 5 153102787 intron variant G/A snv 0.12
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs62398709
rs62398709
5 152675675 intron variant A/T snv 0.34
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement
0.700 1.000 1 2018 2018
dbSNP: rs6867434
rs6867434
1.000 0.040 5 153111474 intron variant T/G snv 0.48
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs6868545
rs6868545
1.000 0.040 5 153115323 intron variant A/C snv 4.0E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 1 2015 2015
dbSNP: rs6886088
rs6886088
1.000 0.040 5 153081231 intron variant C/T snv 0.12
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs6895232
rs6895232
5 152659861 intron variant T/A;C snv
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement
0.700 1.000 1 2018 2018
dbSNP: rs72799107
rs72799107
5 152673844 intron variant C/T snv 0.18
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018