Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9371601
rs9371601
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C0005586
Disease:
Bipolar Disorder 		T 0.820 GeneticVariation GWASCAT Genome-wide association study identifies 30 loci associated with bipolar disorder. 31043756 2019
dbSNP: rs9371601
rs9371601
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C0005586
Disease:
Bipolar Disorder 		0.820 GeneticVariation BEFREE Genome-wide association studies (GWAS) suggest that rs9371601 in the <i>SYNE1</i> gene is a risk SNP for bipolar disorder (BPD) in populations of European ancestry, but further replication analyses across distinct populations are needed. 31236099 2019
dbSNP: rs9371601
rs9371601
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C0005586
Disease:
Bipolar Disorder 		0.820 GeneticVariation GWASDB Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case-control sample. 23070075 2013
dbSNP: rs9371601
rs9371601
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C0005586
Disease:
Bipolar Disorder 		0.820 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs9371601
rs9371601
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C0005586
Disease:
Bipolar Disorder 		0.820 GeneticVariation BEFREE The Psychiatric Genome-Wide Association Study (GWAS) Consortium Bipolar Disorder Working Group (PGC-BD) meta-analysis of BD GWAS data sets and replication samples identified evidence (P=6.7 × 10⁻⁷, odds ratio (OR)=1.147) of association with the risk of BD at the polymorphism rs9371601 within SYNE1, a gene which encodes nesprin-1. 22565781 2013
dbSNP: rs9371601
rs9371601
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C0005586
Disease:
Bipolar Disorder 		T 0.820 GeneticVariation GWASCAT Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4. 21926972 2011
dbSNP: rs9371601
rs9371601
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C0005586
Disease:
Bipolar Disorder 		T 0.820 GeneticVariation GWASDB Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4. 21926972 2011
dbSNP: rs9371601
rs9371601
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C1269683
Disease:
Major Depressive Disorder 		0.800 GeneticVariation GWASDB A mega-analysis of genome-wide association studies for major depressive disorder. 22472876 2013
dbSNP: rs9371601
rs9371601
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C1269683
Disease:
Major Depressive Disorder 		0.800 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs9371601
rs9371601
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder 		0.800 GeneticVariation GWASDB Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs9371601
rs9371601
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C1263846
Disease:
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: rs17082664
rs17082664
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C1269683
Disease:
Major Depressive Disorder 		0.800 GeneticVariation GWASCAT Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. 20351715 2011
dbSNP: rs17082664
rs17082664
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C1269683
Disease:
Major Depressive Disorder 		G 0.800 GeneticVariation GWASDB Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. 20351715 2011
dbSNP: rs119103246
rs119103246
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C2751807
Disease:
Emery-Dreifuss Muscular Dystrophy 4 		T 0.800 CausalMutation CLINVAR
dbSNP: rs119103246
rs119103246
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C2751807
Disease:
Emery-Dreifuss Muscular Dystrophy 4 		0.800 GeneticVariation UNIPROT
dbSNP: rs119103248
rs119103248
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C2751807
Disease:
Emery-Dreifuss Muscular Dystrophy 4 		0.800 GeneticVariation UNIPROT
dbSNP: rs119103248
rs119103248
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C2751807
Disease:
Emery-Dreifuss Muscular Dystrophy 4 		T 0.800 CausalMutation CLINVAR
dbSNP: rs111550108
rs111550108
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs58415480
rs58415480
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C0042133
Disease:
Uterine Fibroids 		C 0.700 GeneticVariation GWASCAT Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. 31649266 2019
dbSNP: rs58415480
rs58415480
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C0042133
Disease:
Uterine Fibroids 		G 0.700 GeneticVariation GWASCAT A Trans-Ethnic Genome-Wide Association Study of Uterine Fibroids. 31249589 2019
dbSNP: rs58415480
rs58415480
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C2242776
Disease:
Plexiform leiomyoma 		C 0.700 GeneticVariation GWASCAT Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. 31649266 2019
dbSNP: rs58415480
rs58415480
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C2242776
Disease:
Plexiform leiomyoma 		G 0.700 GeneticVariation GWASCAT A Trans-Ethnic Genome-Wide Association Study of Uterine Fibroids. 31249589 2019
dbSNP: rs6901631
rs6901631
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C2242776
Disease:
Plexiform leiomyoma 		T 0.700 GeneticVariation GWASCAT Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. 31649266 2019
dbSNP: rs6901631
rs6901631
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C0042133
Disease:
Uterine Fibroids 		T 0.700 GeneticVariation GWASCAT Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. 31649266 2019
dbSNP: rs6904757
rs6904757
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C0042834
Disease:
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019