Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7209436
rs7209436
Entrez Id: 1394;104909134
Gene Symbol: CRHR1;LINC02210-CRHR1
CRHR1;LINC02210-CRHR1
CUI: C0022104
Disease:
Irritable Bowel Syndrome
0.030 GeneticVariation BEFREE Previously, we reported that a CRHR1 gene polymorphism (rs110402, rs242924, and rs7209436) and haplotypes were associated with IBS. 26808377 2016
dbSNP: rs7209436
rs7209436
Entrez Id: 1394;104909134
Gene Symbol: CRHR1;LINC02210-CRHR1
CRHR1;LINC02210-CRHR1
CUI: C0022104
Disease:
Irritable Bowel Syndrome
0.030 GeneticVariation BEFREE The TT genotype of rs7209436 (P = 0.01) and rs242924 (P = 0.02) was significantly more common in patients with IBS than in controls. 22957021 2012
dbSNP: rs7209436
rs7209436
Entrez Id: 1394;104909134
Gene Symbol: CRHR1;LINC02210-CRHR1
CRHR1;LINC02210-CRHR1
CUI: C0022104
Disease:
Irritable Bowel Syndrome
0.030 GeneticVariation BEFREE Three CRH-R1 SNPS (rs110402, rs242924, and rs7209436) were genotyped using salivary DNA from IBS and healthy control subjects (HCs). 27497153 2016
dbSNP: rs12944712
rs12944712
Entrez Id: 1394;104909134
Gene Symbol: CRHR1;LINC02210-CRHR1
CRHR1;LINC02210-CRHR1
CUI: C0038436
Disease:
Post-Traumatic Stress Disorder
0.010 GeneticVariation BEFREE Results indicated that multiple SNPs were associated with acute symptoms at a univariate level, and after correction for multiple testing, rs12944712 was significantly related to acute PTSD symptoms. 21508513 2011
dbSNP: rs12944712
rs12944712
Entrez Id: 1394;104909134
Gene Symbol: CRHR1;LINC02210-CRHR1
CRHR1;LINC02210-CRHR1
CUI: C1269683
Disease:
Major Depressive Disorder
0.010 GeneticVariation BEFREE The sample was subdivided according to sex and smoking status RESULTS: Among nonsmokers, there were nominal associations between MDD and all tested SNPs (rs12944712, P=0.042; rs110402, P=0.031, and rs878886, P=0.040), regardless of sex. 27544317 2016
dbSNP: rs12944712
rs12944712
Entrez Id: 1394;104909134
Gene Symbol: CRHR1;LINC02210-CRHR1
CRHR1;LINC02210-CRHR1
CUI: C0008060
Disease:
child abuse behavior
0.010 GeneticVariation BEFREE FKBP5 (rs1360780) and CRHR1 (rs12944712) polymorphisms significantly interacted with child abuse and adult stress to predict increases in physical health ailments over 3 years. 24099078 2014
dbSNP: rs7209436
rs7209436
Entrez Id: 1394;104909134
Gene Symbol: CRHR1;LINC02210-CRHR1
CRHR1;LINC02210-CRHR1
CUI: C0003469
Disease:
Anxiety Disorders
0.010 GeneticVariation BEFREE We observed interactions between trait anxiety and rs7209436 and rs110402 in CRHR1 in association with baseline cortisol (p LRT = 0.0272 and p LRT = 0.0483, respectively). 23274505 2013
dbSNP: rs7209436
rs7209436
Entrez Id: 1394;104909134
Gene Symbol: CRHR1;LINC02210-CRHR1
CRHR1;LINC02210-CRHR1
CUI: C0003467
Disease:
Anxiety
0.010 GeneticVariation BEFREE We observed interactions between trait anxiety and rs7209436 and rs110402 in CRHR1 in association with baseline cortisol (p LRT = 0.0272 and p LRT = 0.0483, respectively). 23274505 2013
dbSNP: rs7209436
rs7209436
Entrez Id: 1394;104909134
Gene Symbol: CRHR1;LINC02210-CRHR1
CRHR1;LINC02210-CRHR1
CUI: C0016667
Disease:
Fragile X Syndrome
0.010 GeneticVariation BEFREE Results indicate a statistically significant interaction between CRHR1 genotype and the status of raising a child with FXS to predict social anxiety symptoms reported on the SPAI (rs7209436, P = 0.0001). 22573456 2012
dbSNP: rs7209436
rs7209436
Entrez Id: 1394;104909134
Gene Symbol: CRHR1;LINC02210-CRHR1
CRHR1;LINC02210-CRHR1
CUI: C1269683
Disease:
Major Depressive Disorder
0.010 GeneticVariation BEFREE The T-A haplotype consisting of rs7209436 and rs110402 in CRHR1 was positively associated with MDD. 22467522 2012
dbSNP: rs12150390
rs12150390
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0030567
Disease:
Parkinson Disease
0.700 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815 2012
dbSNP: rs1396862
rs1396862
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0030567
Disease:
Parkinson Disease
0.700 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815 2012
dbSNP: rs1396862
rs1396862
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs16940665
rs16940665
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0030567
Disease:
Parkinson Disease
0.700 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815 2012
dbSNP: rs16940665
rs16940665
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs16940665
rs16940665
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0030567
Disease:
Parkinson Disease
0.700 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487 2011
dbSNP: rs16940668
rs16940668
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0030567
Disease:
Parkinson Disease
0.700 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487 2011
dbSNP: rs16940674
rs16940674
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs16940674
rs16940674
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0030567
Disease:
Parkinson Disease
0.700 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487 2011
dbSNP: rs16940676
rs16940676
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0030567
Disease:
Parkinson Disease
0.700 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487 2011
dbSNP: rs16940677
rs16940677
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0030567
Disease:
Parkinson Disease
0.700 GeneticVariation GWASDB Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes. 24842889 2014
dbSNP: rs17425752
rs17425752
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0030567
Disease:
Parkinson Disease
0.700 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487 2011
dbSNP: rs17689471
rs17689471
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs17689653
rs17689653
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs17689824
rs17689824
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012