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: rs10503253
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.850 0.889 4 2011 2017
dbSNP: rs10503256
rs10503256
CSMD1
1.000 0.040 8 4356657 intron variant A/G snv 0.57
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.800 1.000 1 2011 2012
dbSNP: rs10503253
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.700 1.000 1 2013 2013
dbSNP: rs10503253
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2013 2013
dbSNP: rs10503253
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.800 1.000 1 2013 2013
dbSNP: rs10503253
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2013 2013
dbSNP: rs1379326
rs1379326
CSMD1
8 4760288 intron variant T/C;G snv
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial 		0.800 1.000 1 2013 2013
dbSNP: rs4875102
rs4875102
CSMD1
1.000 0.040 8 4427170 intron variant G/A;T snv
CUI: C0158266
Disease: Intervertebral Disc Degeneration
Intervertebral Disc Degeneration 		0.800 1.000 1 2013 2013
dbSNP: rs6558872
rs6558872
CSMD1
0.882 0.040 8 4380617 intron variant G/A;C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2013 2013
dbSNP: rs6558872
rs6558872
CSMD1
0.882 0.040 8 4380617 intron variant G/A;C snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.700 1.000 1 2013 2013
dbSNP: rs6558872
rs6558872
CSMD1
0.882 0.040 8 4380617 intron variant G/A;C snv
CUI: C0036337
Disease: Schizoaffective Disorder
Schizoaffective Disorder 		0.700 1.000 1 2013 2013
dbSNP: rs142700918
rs142700918
CSMD1
0.925 0.080 8 3448320 intron variant G/A snv 5.8E-03
CUI: C0008677
Disease: Bronchitis, Chronic
Bronchitis, Chronic 		0.700 1.000 1 2014 2014
dbSNP: rs142700918
rs142700918
CSMD1
0.925 0.080 8 3448320 intron variant G/A snv 5.8E-03
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.700 1.000 1 2014 2014
dbSNP: rs2688325
rs2688325
CSMD1
8 3909688 intron variant T/C snv 0.63
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2014 2014
dbSNP: rs4395908
rs4395908
CSMD1
1.000 0.120 8 4168122 intron variant C/A;G snv
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis 		0.700 1.000 1 2014 2014
dbSNP: rs73660619
rs73660619
CSMD1
1.000 0.080 8 3230651 intron variant T/C snv 6.8E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.800 1.000 1 2014 2014
dbSNP: rs7463166
rs7463166
CSMD1
8 4976268 intron variant A/G snv 0.26
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2014 2014
dbSNP: rs7828501
rs7828501
CSMD1
8 4702559 intron variant A/G snv 0.48
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2014 2014
dbSNP: rs9987128
rs9987128
CSMD1
1.000 0.040 8 3122601 intron variant A/G snv 0.17
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2015 2015
dbSNP: rs62480124
rs62480124
CSMD1
8 3921114 intron variant G/A;C;T snv
CUI: C4505222
Disease: Sleep Onset Latency
Sleep Onset Latency 		0.700 1.000 1 2016 2016
dbSNP: rs12541020
rs12541020
CSMD1
1.000 0.040 8 4960070 intron variant T/A;C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 2 2017 2019
dbSNP: rs13261217
rs13261217
CSMD1
1.000 0.040 8 4325535 non coding transcript exon variant A/G snv 0.26
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 2 2017 2019
dbSNP: rs11779410
rs11779410
CSMD1 ; LOC105377792
1.000 0.040 8 3015011 intron variant A/T snv 3.2E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs11987640
rs11987640
CSMD1
1.000 8 4584258 intron variant G/C snv 0.12
CUI: C2242776
Disease: Plexiform leiomyoma
Plexiform leiomyoma 		0.700 1.000 1 2017 2017
dbSNP: rs11987640
rs11987640
CSMD1
1.000 8 4584258 intron variant G/C snv 0.12
CUI: C0042133
Disease: Uterine Fibroids
Uterine Fibroids 		0.700 1.000 1 2017 2017