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: 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: 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: 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: 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: 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
dbSNP: rs140364877
rs140364877
MAD1L1 ; LOC100127955 ; MIR4655
1.000 0.040 7 1845542 non coding transcript exon variant C/T snv 4.3E-03
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs140364877
rs140364877
MAD1L1 ; LOC100127955 ; MIR4655
1.000 0.040 7 1845542 non coding transcript exon variant C/T snv 4.3E-03
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: 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: 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: rs12668848
rs12668848
MAD1L1
1.000 0.040 7 1981360 intron variant G/A;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 3 2015 2019
dbSNP: rs10275045
rs10275045
MAD1L1
0.882 0.160 7 1881190 intron variant C/T snv 0.35
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.700 1.000 1 2014 2014
dbSNP: rs10275045
rs10275045
MAD1L1
0.882 0.160 7 1881190 intron variant C/T snv 0.35
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2014 2014
dbSNP: rs12699477
rs12699477
MAD1L1
1.000 0.120 7 1929317 intron variant T/C snv 0.28
CUI: C1336708
Disease: Testicular Germ Cell Tumor
Testicular Germ Cell Tumor 		0.800 1.000 2 2013 2017
dbSNP: rs12699477
rs12699477
MAD1L1
1.000 0.120 7 1929317 intron variant T/C snv 0.28
CUI: C0039590
Disease: Testicular Neoplasms
Testicular Neoplasms 		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: 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: rs6461049
rs6461049
MAD1L1
1.000 0.040 7 1977810 intron variant C/T snv 0.56
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.800 1.000 1 2013 2013
dbSNP: rs12666575
rs12666575
MAD1L1
1.000 0.040 7 1964786 intron variant C/G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.810 1.000 1 2012 2016
dbSNP: rs4721135
rs4721135
MAD1L1
7 1872586 intron variant A/G snv 0.37
CUI: C0023980
Disease: Longevity
Longevity 		0.800 1.000 1 2010 2010