NRXN1, neurexin 1, 9378

N. diseases: 139; N. variants: 41
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1356888
rs1356888
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C0023980
Disease:
Longevity
0.800 GeneticVariation GWASCAT Joint influence of small-effect genetic variants on human longevity. 20834067 2010
dbSNP: rs1356888
rs1356888
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C0023980
Disease:
Longevity
0.800 GeneticVariation GWASDB Joint influence of small-effect genetic variants on human longevity. 20834067 2010
dbSNP: rs1014667
rs1014667
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C0037369
Disease:
Smoking
0.700 GeneticVariation GWASCAT Mercapturic Acids Derived from the Toxicants Acrolein and Crotonaldehyde in the Urine of Cigarette Smokers from Five Ethnic Groups with Differing Risks for Lung Cancer. 26053186 2015
dbSNP: rs1014667
rs1014667
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C1519383
Disease:
Smoking Behaviors
0.700 GeneticVariation GWASCAT Mercapturic Acids Derived from the Toxicants Acrolein and Crotonaldehyde in the Urine of Cigarette Smokers from Five Ethnic Groups with Differing Risks for Lung Cancer. 26053186 2015
dbSNP: rs10490165
rs10490165
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C0027404
Disease:
Narcolepsy
0.700 GeneticVariation GWASDB Genome-wide association database developed in the Japanese Integrated Database Project. 19629137 2009
dbSNP: rs10490175
rs10490175
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C0021704
Disease:
Intelligence
0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203 2019
dbSNP: rs10490175
rs10490175
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C0036341
Disease:
Schizophrenia
0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203 2019
dbSNP: rs12618157
rs12618157
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C0002736
Disease:
Amyotrophic Lateral Sclerosis
0.700 GeneticVariation GWASDB Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. 17362836 2007
dbSNP: rs141864436
rs141864436
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation GWASCAT Genetic Variants in HSD17B3, SMAD3, and IPO11 Impact Circulating Lipids in Response to Fenofibrate in Individuals With Type 2 Diabetes. 28736931 2018
dbSNP: rs141864436
rs141864436
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C3894553
Disease:
response to simvastatin
0.700 GeneticVariation GWASCAT Genetic Variants in HSD17B3, SMAD3, and IPO11 Impact Circulating Lipids in Response to Fenofibrate in Individuals With Type 2 Diabetes. 28736931 2018
dbSNP: rs2059308
rs2059308
Entrez Id: 9378;101927089
Gene Symbol: NRXN1;LOC101927089
NRXN1;LOC101927089
CUI: C1305855
Disease:
Body mass index
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs41522849
rs41522849
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C0410702
Disease:
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: rs41522849
rs41522849
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C1837461
Disease:
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: rs9636391
rs9636391
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C1305855
Disease:
Body mass index
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs10187911
rs10187911
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C0684249
Disease:
Carcinoma of lung
0.010 GeneticVariation BEFREE For external validation, nineteen SNPs were replicated in another sample set composed of 293 cases and 495 controls, and only rs10187911 on 2p16.3 was significantly associated with lung cancer development (dominant model, OR of TG or GG, 1.58, P = 0.025). 23772147 2013
dbSNP: rs10187911
rs10187911
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C1306460
Disease:
Primary malignant neoplasm of lung
0.010 GeneticVariation BEFREE For external validation, nineteen SNPs were replicated in another sample set composed of 293 cases and 495 controls, and only rs10187911 on 2p16.3 was significantly associated with lung cancer development (dominant model, OR of TG or GG, 1.58, P = 0.025). 23772147 2013
dbSNP: rs10187911
rs10187911
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C0242379
Disease:
Malignant neoplasm of lung
0.010 GeneticVariation BEFREE For external validation, nineteen SNPs were replicated in another sample set composed of 293 cases and 495 controls, and only rs10187911 on 2p16.3 was significantly associated with lung cancer development (dominant model, OR of TG or GG, 1.58, P = 0.025). 23772147 2013
dbSNP: rs1045881
rs1045881
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C0036341
Disease:
Schizophrenia
0.010 GeneticVariation BEFREE The rs1045881 variant was not significantly associated with schizophrenia (N=302 case-control pairs), but with clozapine response (N=163; p=0.030). 21890328 2011
dbSNP: rs10490162
rs10490162
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C0036341
Disease:
Schizophrenia
0.010 GeneticVariation BEFREE Based on previous suggestive evidence of an impact on clozapine response in patients with schizophrenia, we conducted an association study of NRXN1 polymorphisms (rs12467557 and rs10490162) with antipsychotic treatment response in 54 patients with schizophrenia in a double blind, placebo-controlled NIMH inpatient crossover trial and examined for association with risk for schizophrenia in independent case-control and family-based clinical cohorts. 24633560 2014
dbSNP: rs10490168
rs10490168
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C0036341
Disease:
Schizophrenia
0.010 GeneticVariation BEFREE Our results showed that four SNPs of NRXN1 gene were significantly associated with schizophrenia (rs10490168: G > A, p = 0.017; rs2024513: A > G, p = 0.006; rs13382584: T > C, p = 0.009; and rs1558852: G > A, p = 0.031). 21477380 2011
dbSNP: rs10865246
rs10865246
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C0028043
Disease:
Nicotine Dependence
0.010 GeneticVariation BEFREE Two SNPs in NRXN1 and two in CHRNA5 were associated with cigarette consumption, while rs10865246/C (NRXN1) was associated with high nicotine addiction. 27355804 2016
dbSNP: rs112638127
rs112638127
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C0036341
Disease:
Schizophrenia
0.010 GeneticVariation BEFREE Since I1068V was observed in a single patient, it is impossible to exclude the possibility that I1068V makes a minor contribution to schizophrenia susceptibility. 21288692 2011
dbSNP: rs12467557
rs12467557
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C0036341
Disease:
Schizophrenia
0.010 GeneticVariation BEFREE Based on previous suggestive evidence of an impact on clozapine response in patients with schizophrenia, we conducted an association study of NRXN1 polymorphisms (rs12467557 and rs10490162) with antipsychotic treatment response in 54 patients with schizophrenia in a double blind, placebo-controlled NIMH inpatient crossover trial and examined for association with risk for schizophrenia in independent case-control and family-based clinical cohorts. 24633560 2014
dbSNP: rs13382584
rs13382584
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C0036341
Disease:
Schizophrenia
0.010 GeneticVariation BEFREE Our results showed that four SNPs of NRXN1 gene were significantly associated with schizophrenia (rs10490168: G > A, p = 0.017; rs2024513: A > G, p = 0.006; rs13382584: T > C, p = 0.009; and rs1558852: G > A, p = 0.031). 21477380 2011
dbSNP: rs1421589
rs1421589
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C0019569
Disease:
Hirschsprung Disease
0.010 GeneticVariation BEFREE Several SNPs were significantly associated with altered risk of HD in the Chinese Han population, including rs1421589 within <i>NRXN1</i>, rs11795613 and rs4844285 within <i>NLGN3,</i> as well as rs5961397, rs7157669 and rs724373 within <i>NLGX4X</i> (all P<0.05). 29622757 2018