NRXN3, neurexin 3, 9369

N. diseases: 64; N. variants: 29
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1004212
rs1004212
Entrez Id: 9369
Gene Symbol: NRXN3
NRXN3
CUI: C0549393
Disease:
Alcohol problem
0.010 GeneticVariation BEFREE In men, there were modest associations between rs11624704 and attentional impulsivity (p=0.005) and between rs1004212 and alcohol problems (p=0.009). 21676558 2011
dbSNP: rs1004212
rs1004212
Entrez Id: 9369
Gene Symbol: NRXN3
NRXN3
CUI: C0021125
Disease:
Impulsive Behavior
0.010 GeneticVariation BEFREE In men, there were modest associations between rs11624704 and attentional impulsivity (p=0.005) and between rs1004212 and alcohol problems (p=0.009). 21676558 2011
dbSNP: rs10083466
rs10083466
Entrez Id: 9369
Gene Symbol: NRXN3
NRXN3
CUI: C0006012
Disease:
Borderline Personality Disorder
0.010 GeneticVariation BEFREE The strongest association with screening positive for BPD was found for the NRXN3 SNP, rs10083466 (p=.0013). 23245376 2013
dbSNP: rs10146997
rs10146997
Entrez Id: 9369
Gene Symbol: NRXN3
NRXN3
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE Moreover, G allele carriers in rs10146997 of the NRXN3 gene were the youngest patients at onset of breast cancer</span>. 21688152 2012
dbSNP: rs10146997
rs10146997
Entrez Id: 9369
Gene Symbol: NRXN3
NRXN3
CUI: C0008350
Disease:
Cholelithiasis
0.010 GeneticVariation BEFREE The MC4R(rs17782313) (OR 1.27, 95% CI [1.02;1.58]), MAP2K5(rs2241423) (OR 1.80, 95% CI [1.04;3.41]), NRXN3(rs10146997) (OR 1.26, 95% CI [1.01;1.57]), HHEX(rs1111875) (OR 1.29, 95% CI [1.03;1.62]), FAIM2(rs7138803) (OR 0.66, 95% CI [0.48;0.91]), and apolipoprotein E4 allele (OR 0.76, 95% CI [0.59;0.98]) were associated with gallstone disease. 28799434 2017
dbSNP: rs10146997
rs10146997
Entrez Id: 9369
Gene Symbol: NRXN3
NRXN3
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE Moreover, G allele carriers in rs10146997 of the NRXN3 gene were the youngest patients at onset of breast cancer</span>. 21688152 2012
dbSNP: rs10146997
rs10146997
Entrez Id: 9369
Gene Symbol: NRXN3
NRXN3
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE The minor G-allele of rs10146997 in NRXN3 associated with increased WC among women (β = 0.55cm (0.20;0.89), p(additive) = 1.7×10(-3), p(interaction) = 1.0×10(-3)), but showed no associations with obesity related metabolic traits. 21674055 2011
dbSNP: rs11624704
rs11624704
Entrez Id: 9369
Gene Symbol: NRXN3
NRXN3
CUI: C0549393
Disease:
Alcohol problem
0.010 GeneticVariation BEFREE In men, there were modest associations between rs11624704 and attentional impulsivity (p=0.005) and between rs1004212 and alcohol problems (p=0.009). 21676558 2011
dbSNP: rs11624704
rs11624704
Entrez Id: 9369
Gene Symbol: NRXN3
NRXN3
CUI: C0021125
Disease:
Impulsive Behavior
0.010 GeneticVariation BEFREE In men, there were modest associations between rs11624704 and attentional impulsivity (p=0.005) and between rs1004212 and alcohol problems (p=0.009). 21676558 2011
dbSNP: rs2217887
rs2217887
Entrez Id: 9369
Gene Symbol: NRXN3
NRXN3
CUI: C0853193
Disease:
Bipolar I disorder
0.010 GeneticVariation BEFREE For markers genotyped in replication samples, rs7619173 exhibited a significant association (P(combined) = 2 ∗ 10(-4)) after multiple testing correction, while markers rs11001178 (MYST4) and rs2217887 (NRXN3) showed weak associations (P(combined) = 0.02) with BPD-I. 24444492 2014
dbSNP: rs3850370
rs3850370
Entrez Id: 9369
Gene Symbol: NRXN3
NRXN3
CUI: C0007131
Disease:
Non-Small Cell Lung Carcinoma
0.010 GeneticVariation BEFREE The minor allele of three SNPs (rs7629386 at 3p22.1, rs969088 at 5p14.1, and rs3850370 at 14q24.3) were associated with worse NSCLC survival while 2 (rs41997 at 7q31.31 and rs12000445 at 9p21.3) were associated with better NSCLC survival. 22872573 2012
dbSNP: rs7154021
rs7154021
Entrez Id: 9369
Gene Symbol: NRXN3
NRXN3
CUI: C0036341
Disease:
Schizophrenia
0.010 GeneticVariation BEFREE Several haplotypes were significantly associated with schizophrenia, constructed by rs11624704-rs7157669-rs724373 (AAC, p=0.003; ACT, p=0.007, both remained significant after permutation tests), rs7154021-rs7142344 (TT, p=0.024; CT, p=0.012), respectively. 23306218 2013
dbSNP: rs7157669
rs7157669
Entrez Id: 9369
Gene Symbol: NRXN3
NRXN3
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
dbSNP: rs7157669
rs7157669
Entrez Id: 9369
Gene Symbol: NRXN3
NRXN3
CUI: C0036341
Disease:
Schizophrenia
0.010 GeneticVariation BEFREE Our results showed that three SNPs were associated with schizophrenia (rs7157669: A>C, p=0.006; rs724373: C>T, p=0.014; rs7154021: C>T, p=0.018). 23306218 2013
dbSNP: rs724373
rs724373
Entrez Id: 9369
Gene Symbol: NRXN3
NRXN3
CUI: C0036341
Disease:
Schizophrenia
0.010 GeneticVariation BEFREE Our results showed that three SNPs were associated with schizophrenia (rs7157669: A>C, p=0.006; rs724373: C>T, p=0.014; rs7154021: C>T, p=0.018). 23306218 2013
dbSNP: rs724373
rs724373
Entrez Id: 9369
Gene Symbol: NRXN3
NRXN3
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
dbSNP: rs8019381
rs8019381
Entrez Id: 9369
Gene Symbol: NRXN3
NRXN3
CUI: C0002395
Disease:
Alzheimer's Disease
0.010 GeneticVariation BEFREE We found that the SNP rs8019381 of NRXN3 that is located adjacent to splicing site #5 (SS#5) interacts with the APOE ε4 haplotype and alters NRXN3 transmembrane or soluble isoform expression in AD postmortem cortex. 30902061 2019
dbSNP: rs1057519451
rs1057519451
Entrez Id: 9369;105370589
Gene Symbol: NRXN3;LOC105370589
NRXN3;LOC105370589
CUI: C0349588
Disease:
Short stature
G 0.700 CausalMutation CLINVAR
dbSNP: rs1057519451
rs1057519451
Entrez Id: 9369;105370589
Gene Symbol: NRXN3;LOC105370589
NRXN3;LOC105370589
CUI: C1849075
Disease:
Relative macrocephaly
G 0.700 CausalMutation CLINVAR
dbSNP: rs531047390
rs531047390
Entrez Id: 9369
Gene Symbol: NRXN3
NRXN3
CUI: C1849075
Disease:
Relative macrocephaly
G 0.700 CausalMutation CLINVAR
dbSNP: rs531047390
rs531047390
Entrez Id: 9369
Gene Symbol: NRXN3
NRXN3
CUI: C0349588
Disease:
Short stature
G 0.700 CausalMutation CLINVAR
dbSNP: rs10146997
rs10146997
Entrez Id: 9369
Gene Symbol: NRXN3
NRXN3
CUI: C0455829
Disease:
Waist Circumference
G 0.800 GeneticVariation GWASCAT In stage 1, 31,373 individuals of Caucasian descent from eight cohort studies confirmed the role of FTO and MC4R and identified one novel locus associated with WC in the neurexin 3 gene [NRXN3 (rs10146997, p = 6.4x10(-7))]. 19557197 2009
dbSNP: rs11624704
rs11624704
Entrez Id: 9369
Gene Symbol: NRXN3
NRXN3
CUI: C0028754
Disease:
Obesity
0.800 GeneticVariation GWASCAT We next examined obesity-related quantitative traits (such as total body weight, waist circumference and waist to hip ratio), and detected genome-wide significant signals between waist to hip ratio and NRXN3 (rs11624704, P = 2.67 × 10(-9)), previously associated with body weight and fat distribution. 21552555 2011
dbSNP: rs2370983
rs2370983
Entrez Id: 9369
Gene Symbol: NRXN3
NRXN3
CUI: C0028754
Disease:
Obesity
A 0.800 GeneticVariation GWASCAT Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. 23563607 2013
dbSNP: rs7141420
rs7141420
Entrez Id: 9369
Gene Symbol: NRXN3
NRXN3
CUI: C0028754
Disease:
Obesity
T 0.800 GeneticVariation GWASCAT Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. 23563607 2013