SATB2, SATB homeobox 2, 23314

N. diseases: 233; N. variants: 38
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6704641
rs6704641
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C0036341
Disease:
Schizophrenia 		0.710 GeneticVariation GWASCAT Association of Schizophrenia Risk With Disordered Niacin Metabolism in an Indian Genome-wide Association Study. 31268507 2019
dbSNP: rs6704641
rs6704641
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C0036341
Disease:
Schizophrenia 		0.710 GeneticVariation BEFREE We found that rs6704641 was significantly associated with schizophrenia in both allelic and genotypic distributions (Pallele = 0.008, Pgenotype = 0.028 after correction). 31162297 2019
dbSNP: rs6704641
rs6704641
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C0036341
Disease:
Schizophrenia 		A 0.710 GeneticVariation GWASCAT Genome-wide association study of schizophrenia in Ashkenazi Jews. 26198764 2015
dbSNP: rs6704641
rs6704641
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C0036341
Disease:
Schizophrenia 		A 0.710 GeneticVariation GWASCAT Biological insights from 108 schizophrenia-associated genetic loci. 25056061 2014
dbSNP: rs114693875
rs114693875
Entrez Id: 23314;150538
Gene Symbol: SATB2;SATB2-AS1
SATB2;SATB2-AS1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs895526
rs895526
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C0036341
Disease:
Schizophrenia 		C 0.700 GeneticVariation GWASCAT Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect. 30285260 2019
dbSNP: rs13014796
rs13014796
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C0596887
Disease:
mathematical ability 		A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs17196295
rs17196295
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C0003467
Disease:
Anxiety 		G 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs17266097
rs17266097
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C0596887
Disease:
mathematical ability 		T 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs1057518496
rs1057518496
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C0026827
Disease:
Muscle hypotonia 		A 0.700 CausalMutation CLINVAR Clinical and molecular consequences of disease-associated de novo mutations in SATB2. 28151491 2017
dbSNP: rs1057518496
rs1057518496
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C0026827
Disease:
Muscle hypotonia 		A 0.700 CausalMutation CLINVAR A de novo SATB2 mutation in monozygotic twins with cleft palate, dental anomalies, and developmental delay. 28211976 2017
dbSNP: rs1057518496
rs1057518496
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C0432072
Disease:
Dysmorphic features 		A 0.700 CausalMutation CLINVAR DEPDC5 mutations in familial and sporadic focal epilepsy. 28170089 2017
dbSNP: rs1057518496
rs1057518496
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C0432072
Disease:
Dysmorphic features 		A 0.700 CausalMutation CLINVAR Clinical and molecular consequences of disease-associated de novo mutations in SATB2. 28151491 2017
dbSNP: rs1057518496
rs1057518496
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C0432072
Disease:
Dysmorphic features 		A 0.700 CausalMutation CLINVAR A de novo SATB2 mutation in monozygotic twins with cleft palate, dental anomalies, and developmental delay. 28211976 2017
dbSNP: rs1057518496
rs1057518496
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C0026827
Disease:
Muscle hypotonia 		A 0.700 CausalMutation CLINVAR Genotype and phenotype in 12 additional individuals with SATB2-associated syndrome. 28139846 2017
dbSNP: rs1057518496
rs1057518496
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C0026827
Disease:
Muscle hypotonia 		A 0.700 CausalMutation CLINVAR DEPDC5 mutations in familial and sporadic focal epilepsy. 28170089 2017
dbSNP: rs1057518496
rs1057518496
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C0432072
Disease:
Dysmorphic features 		A 0.700 CausalMutation CLINVAR Genotype and phenotype in 12 additional individuals with SATB2-associated syndrome. 28139846 2017
dbSNP: rs1057521083
rs1057521083
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C0026650
Disease:
Movement Disorders 		A 0.700 GeneticVariation CLINVAR DEPDC5 mutations in familial and sporadic focal epilepsy. 28170089 2017
dbSNP: rs1057521083
rs1057521083
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C0432072
Disease:
Dysmorphic features 		A 0.700 GeneticVariation CLINVAR DEPDC5 mutations in familial and sporadic focal epilepsy. 28170089 2017
dbSNP: rs1057521083
rs1057521083
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C0026650
Disease:
Movement Disorders 		A 0.700 GeneticVariation CLINVAR Genotype and phenotype in 12 additional individuals with SATB2-associated syndrome. 28139846 2017
dbSNP: rs1057521083
rs1057521083
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C0000772
Disease:
Multiple congenital anomalies 		A 0.700 GeneticVariation CLINVAR Clinical and molecular consequences of disease-associated de novo mutations in SATB2. 28151491 2017
dbSNP: rs1057521083
rs1057521083
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C0000772
Disease:
Multiple congenital anomalies 		A 0.700 GeneticVariation CLINVAR DEPDC5 mutations in familial and sporadic focal epilepsy. 28170089 2017
dbSNP: rs1057521083
rs1057521083
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C0432072
Disease:
Dysmorphic features 		A 0.700 GeneticVariation CLINVAR Genotype and phenotype in 12 additional individuals with SATB2-associated syndrome. 28139846 2017
dbSNP: rs1057521083
rs1057521083
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C2676739
Disease:
Chromosome 2q32-Q33 Deletion Syndrome 		A 0.700 CausalMutation CLINVAR Clinical and molecular consequences of disease-associated de novo mutations in SATB2. 28151491 2017
dbSNP: rs1057521083
rs1057521083
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C0432072
Disease:
Dysmorphic features 		A 0.700 GeneticVariation CLINVAR A de novo SATB2 mutation in monozygotic twins with cleft palate, dental anomalies, and developmental delay. 28211976 2017