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: 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: 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: rs4721135
rs4721135
MAD1L1
7 1872586 intron variant A/G snv 0.37
CUI: C0023980
Disease: Longevity
Longevity 		0.800 1.000 1 2010 2010
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: 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: rs4721089
rs4721089
MAD1L1
7 1833285 intron variant C/T snv 0.80
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2019 2019
dbSNP: rs58120505
rs58120505
MAD1L1
1.000 0.040 7 1990232 intron variant T/C snv 0.37
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 2 2019 2019
dbSNP: rs10267593
rs10267593
MAD1L1
1.000 0.040 7 1897625 intron variant G/A snv 0.25
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018
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: rs10650434
rs10650434
MAD1L1
1.000 0.040 7 1985461 intron variant -/TC delins 0.57
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2018 2018
dbSNP: rs10950456
rs10950456
MAD1L1
1.000 0.040 7 1940114 5 prime UTR variant G/A snv 0.57
CUI: C0236773
Disease: Depressed bipolar I disorder
Depressed bipolar I disorder 		0.700 1.000 1 2019 2019
dbSNP: rs11514731
rs11514731
MAD1L1
1.000 0.040 7 2011868 intron variant C/G snv 0.16
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs11514731
rs11514731
MAD1L1
1.000 0.040 7 2011868 intron variant C/G snv 0.16
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs11763750
rs11763750
MAD1L1
7 2040479 intron variant G/A snv 0.16
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 1 2019 2019
dbSNP: rs11770148
rs11770148
MAD1L1
7 1859811 intron variant A/G;T snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs11772232
rs11772232
MAD1L1 ; LOC105375128
7 1816637 intron variant C/T snv 0.13
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs117829095
rs117829095
MAD1L1
7 1892738 intron variant C/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
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: rs13234909
rs13234909
MAD1L1
7 1827295 intron variant G/A snv 0.33
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs13240401
rs13240401
MAD1L1
7 2154761 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: rs1860826
rs1860826
MAD1L1
7 2072871 intron variant G/A;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2019 2019
dbSNP: rs2056477
rs2056477
MAD1L1
1.000 0.040 7 2040109 intron variant G/A;C;T snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018