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: rs34731055
rs34731055
MAD1L1
7 2067293 intron variant C/T snv 0.13
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 1 2019 2019
dbSNP: rs34782622
rs34782622
MAD1L1
7 2155497 intron variant A/G snv 0.14
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs3800917
rs3800917
MAD1L1
1.000 7 2128304 intron variant G/A snv 0.28
CUI: C0869220
Disease: Adverse effects, not elsewhere classified
Adverse effects, not elsewhere classified 		0.700 1.000 1 2019 2019
dbSNP: rs3823624
rs3823624
MAD1L1
1.000 0.040 7 2070711 intron variant T/C snv 0.17
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2019 2019
dbSNP: rs3823624
rs3823624
MAD1L1
1.000 0.040 7 2070711 intron variant T/C snv 0.17
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 1 2019 2019
dbSNP: rs3931398
rs3931398
MAD1L1
1.000 0.040 7 1991957 intron variant G/A snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs3996330
rs3996330
MAD1L1
7 1979188 intron variant C/A snv 0.54
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs4236274
rs4236274
MAD1L1
1.000 0.040 7 1856777 intron variant A/G snv 0.47
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.700 1.000 1 2016 2016
dbSNP: rs4332037
rs4332037
MAD1L1
1.000 0.040 7 1911173 intron variant C/T snv 0.19
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs4721096
rs4721096
MAD1L1 ; LOC100127955
1.000 0.040 7 1837675 intron variant T/C snv 0.84
CUI: C0017168
Disease: Gastroesophageal reflux disease
Gastroesophageal reflux disease 		0.700 1.000 1 2019 2019
dbSNP: rs4721295
rs4721295
MAD1L1
0.882 0.040 7 1997034 intron variant T/G snv 0.33
CUI: C0036337
Disease: Schizoaffective Disorder
Schizoaffective Disorder 		0.700 1.000 1 2013 2013
dbSNP: rs4721295
rs4721295
MAD1L1
0.882 0.040 7 1997034 intron variant T/G snv 0.33
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2013 2013
dbSNP: rs4721295
rs4721295
MAD1L1
0.882 0.040 7 1997034 intron variant T/G snv 0.33
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.700 1.000 1 2013 2013
dbSNP: rs527510716
rs527510716
MAD1L1
1.000 0.080 7 1904901 intron variant G/C snv 0.14
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.700 1.000 1 2018 2018
dbSNP: rs56072378
rs56072378
MAD1L1
1.000 0.040 7 2064729 intron variant A/G snv 0.29
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs57633152
rs57633152
MAD1L1
7 2002912 intron variant C/G snv 0.46
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs58120505
rs58120505
MAD1L1
1.000 0.040 7 1990232 intron variant T/C snv 0.37
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs59574136
rs59574136
MAD1L1
1.000 0.040 7 1996825 intron variant T/C snv 0.10
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2017 2017
dbSNP: rs59574136
rs59574136
MAD1L1
1.000 0.040 7 1996825 intron variant T/C snv 0.10
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs62442924
rs62442924
MAD1L1
7 1950341 intron variant C/T snv 0.17
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs6963853
rs6963853
MAD1L1 ; LOC105375128
7 1819089 intron variant G/A snv 0.48
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs71525361
rs71525361
MAD1L1
7 2120142 intron variant T/A;C snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018