Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10503253
rs10503253
CSMD1
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		A 0.850 GeneticVariation GWASCAT Genome-wide association study of schizophrenia in Ashkenazi Jews. 26198764

2015
dbSNP: rs10503253
rs10503253
CSMD1
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		A 0.850 GeneticVariation GWASCAT Biological insights from 108 schizophrenia-associated genetic loci. 25056061

2014
dbSNP: rs10503253
rs10503253
CSMD1
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.850 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885

2013
dbSNP: rs10503253
rs10503253
CSMD1
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		A 0.850 GeneticVariation GWASCAT Genome-wide association study identifies five new schizophrenia loci. 21926974

2011
dbSNP: rs10503253
rs10503253
CSMD1
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.800 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885

2013
dbSNP: rs10503256
rs10503256
CSMD1
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.800 GeneticVariation GWASCAT Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder. 22688191

2012
dbSNP: rs1379326
rs1379326
CSMD1
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial 		C 0.800 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis. 23583980

2013
dbSNP: rs4875102
rs4875102
CSMD1
CUI: C0158266
Disease: Intervertebral Disc Degeneration
Intervertebral Disc Degeneration 		A 0.800 GeneticVariation GWASCAT Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects. 22993228

2013
dbSNP: rs73660619
rs73660619
CSMD1
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.800 GeneticVariation GWASCAT Genome-wide association study of the rate of cognitive decline in Alzheimer's disease. 23535033

2014
dbSNP: rs10046758
rs10046758
CSMD1
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 GeneticVariation GWASCAT Association of Schizophrenia Risk With Disordered Niacin Metabolism in an Indian Genome-wide Association Study. 31268507

2019
dbSNP: rs10503253
rs10503253
CSMD1
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885

2013
dbSNP: rs10503253
rs10503253
CSMD1
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885

2013
dbSNP: rs10503253
rs10503253
CSMD1
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.700 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885

2013
dbSNP: rs11136775
rs11136775
CSMD1
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117

2018
dbSNP: rs11136775
rs11136775
CSMD1
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117

2018
dbSNP: rs11779410
rs11779410
CSMD1 ; LOC105377792
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017
dbSNP: rs11787412
rs11787412
CSMD1
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese. 31417091

2019
dbSNP: rs11787412
rs11787412
CSMD1
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese. 31417091

2019
dbSNP: rs11987640
rs11987640
CSMD1
CUI: C2242776
Disease: Plexiform leiomyoma
Plexiform leiomyoma 		G 0.700 GeneticVariation GWASCAT A multi-stage genome-wide association study of uterine fibroids in African Americans. 28836065

2017
dbSNP: rs11987640
rs11987640
CSMD1
CUI: C0042133
Disease: Uterine Fibroids
Uterine Fibroids 		G 0.700 GeneticVariation GWASCAT A multi-stage genome-wide association study of uterine fibroids in African Americans. 28836065

2017
dbSNP: rs11998250
rs11998250
CSMD1
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017
dbSNP: rs12541020
rs12541020
CSMD1
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		T 0.700 GeneticVariation GWASCAT Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect. 30285260

2019
dbSNP: rs12541020
rs12541020
CSMD1
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		T 0.700 GeneticVariation GWASCAT Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia. 28991256

2017
dbSNP: rs12550650
rs12550650
CSMD1
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs13250365
rs13250365
CSMD1
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017