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: 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: 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: 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: 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: 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: rs1658820
rs1658820
CSMD1
8 4431055 intron variant G/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2019 2019
dbSNP: rs10046758
rs10046758
CSMD1
1.000 0.040 8 4326648 non coding transcript exon variant C/G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2019 2019
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: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2013 2013
dbSNP: rs11136775
rs11136775
CSMD1
0.925 0.040 8 4791194 intron variant G/C snv 0.12
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs11136775
rs11136775
CSMD1
0.925 0.040 8 4791194 intron variant G/C snv 0.12
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
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: rs11787412
rs11787412
CSMD1
0.925 0.040 8 3276717 intron variant C/A;T snv
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2019 2019
dbSNP: rs11787412
rs11787412
CSMD1
0.925 0.040 8 3276717 intron variant C/A;T snv
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2019 2019
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
dbSNP: rs11998250
rs11998250
CSMD1
1.000 0.040 8 3162070 intron variant A/C snv 0.22
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs12550650
rs12550650
CSMD1
8 4693468 intron variant C/T snv 0.49
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2019 2019
dbSNP: rs13250365
rs13250365
CSMD1
1.000 0.040 8 3155942 intron variant G/C;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs13260434
rs13260434
CSMD1
0.925 0.040 8 3368702 intron variant T/A snv 0.24
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs13260434
rs13260434
CSMD1
0.925 0.040 8 3368702 intron variant T/A snv 0.24
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018