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: 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: 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: 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: rs2627395
rs2627395
CSMD1
8 3921330 intron variant C/T snv 0.58
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		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: 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: rs4633074
rs4633074
CSMD1
8 4924352 intron variant G/A;C;T snv
CUI: C0005890
Disease: Body Height
Body Height 		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
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: 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
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: 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: rs2046197
rs2046197
CSMD1
1.000 0.080 8 3762230 intron variant G/A;C;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2018 2018
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: rs73505850
rs73505850
CSMD1
1.000 0.040 8 4897316 intron variant G/A snv 2.4E-02
CUI: C0024530
Disease: Malaria
Malaria 		0.700 1.000 1 2018 2018
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
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