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: rs139425113
rs139425113
CSMD1
1.000 0.040 8 4323090 intron variant A/-;AA;AAA delins
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2018 2018
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: 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: 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: rs145669495
rs145669495
CSMD1
8 4244902 intron variant A/G snv 1.6E-03
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE 		0.700 1.000 1 2017 2017
dbSNP: rs4266671
rs4266671
CSMD1
8 4971671 intron variant A/G snv 0.27
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2019 2019
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: rs17404163
rs17404163
CSMD1
8 4093523 intron variant A/G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		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: rs4876060
rs4876060
CSMD1 ; LOC105377792
1.000 0.040 8 3013377 intron variant A/T snv 7.0E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
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: 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: 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: 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: rs2688326
rs2688326
CSMD1
8 3910101 intron variant C/A;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2019 2019
dbSNP: rs67121641
rs67121641
CSMD1
8 4936142 intron variant C/G snv 0.26
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs673465
rs673465
CSMD1 ; LOC105377792
1.000 0.040 8 3000838 intron variant C/G snv 0.87
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
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: rs78686130
rs78686130
CSMD1
8 4270789 intron variant C/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019