rs2910709
×
Entrez Id:
100861519
Gene Symbol:
GDNF-AS1
GDNF-AS1
Heroin Dependence
0.010
GeneticVariation
BEFREE
An increased risk of HD and depression was associated with rs2910709 T/T genotype and rs884344 C allele, respectively, suggesting GDNF is a novel susceptibility gene for depression and HD .
24022000
2013
rs2910709
×
Entrez Id:
100861519
Gene Symbol:
GDNF-AS1
GDNF-AS1
Depressed mood
0.010
GeneticVariation
BEFREE
An increased risk of HD and depression was associated with rs2910709 T/T genotype and rs884344 C allele, respectively, suggesting GDNF is a novel susceptibility gene for depression and HD.
24022000
2013
rs2910709
×
Entrez Id:
100861519
Gene Symbol:
GDNF-AS1
GDNF-AS1
Mental Depression
0.010
GeneticVariation
BEFREE
An increased risk of HD and depression was associated with rs2910709 T/T genotype and rs884344 C allele, respectively, suggesting GDNF is a novel susceptibility gene for depression and HD.
24022000
2013
rs2910709
×
Entrez Id:
100861519
Gene Symbol:
GDNF-AS1
GDNF-AS1
Depressive disorder
0.010
GeneticVariation
BEFREE
An increased risk of HD and depression was associated with rs2910709 T/T genotype and rs884344 C allele, respectively, suggesting GDNF is a novel susceptibility gene for depression and HD.
24022000
2013
rs4574573
GDNF-AS1;LINC02117
Serum total cholesterol measurement
0.700
GeneticVariation
GWASCAT
Very low-depth whole-genome sequencing in complex trait association studies.
30576415
2019
rs104893891
GDNF;GDNF-AS1
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
0.800
GeneticVariation
UNIPROT
Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient.
8896568
1996
rs104893891
GDNF;GDNF-AS1
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
0.800
GeneticVariation
UNIPROT
De novo mutation of GDNF, ligand for the RET/GDNFR-alpha receptor complex, in Hirschsprung disease.
8968758
1996
rs104893891
GDNF;GDNF-AS1
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
0.800
GeneticVariation
UNIPROT
Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease.
8896569
1996
rs104893891
GDNF;GDNF-AS1
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
0.800
GeneticVariation
UNIPROT
Pathogenesis of Hirschsprung's disease.
10917288
2000
rs104893891
GDNF;GDNF-AS1
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
A
0.800
SusceptibilityMutation
CLINVAR
rs121918536
GDNF;GDNF-AS1
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
0.800
GeneticVariation
UNIPROT
Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease.
8896569
1996
rs121918536
GDNF;GDNF-AS1
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
C
0.800
SusceptibilityMutation
CLINVAR
rs121918536
GDNF;GDNF-AS1
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
0.800
GeneticVariation
UNIPROT
Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient.
8896568
1996
rs121918536
GDNF;GDNF-AS1
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
0.800
GeneticVariation
UNIPROT
Pathogenesis of Hirschsprung's disease.
10917288
2000
rs121918536
GDNF;GDNF-AS1
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
0.800
GeneticVariation
UNIPROT
De novo mutation of GDNF, ligand for the RET/GDNFR-alpha receptor complex, in Hirschsprung disease.
8968758
1996
rs36119840
GDNF;GDNF-AS1
Pheochromocytoma
0.710
GeneticVariation
BEFREE
No GDNF mutations were identified in patients with familial phaeochromocytoma disease, but a c277C-->T (R93W ) sequence variant was identified in one of 28 sporadic tumours.
9215674
1997
rs36119840
GDNF;GDNF-AS1
Pheochromocytoma
0.710
GeneticVariation
UNIPROT
No GDNF mutations were identified in patients with familial phaeochromocytoma disease, but a c277C-->T (R93W ) sequence variant was identified in one of 28 sporadic tumours.
9215674
1997
rs11747340
GDNF;GDNF-AS1
Blood Protein Measurement
A
0.700
GeneticVariation
GWASCAT
Genome and epigenome wide studies of neurological protein biomarkers in the Lothian Birth Cohort 1936.
31320639
2019
rs36119840
GDNF;GDNF-AS1
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
0.700
GeneticVariation
UNIPROT
Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease.
8896569
1996
rs36119840
GDNF;GDNF-AS1
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
0.700
GeneticVariation
UNIPROT
De novo mutation of GDNF, ligand for the RET/GDNFR-alpha receptor complex, in Hirschsprung disease.
8968758
1996
rs36119840
GDNF;GDNF-AS1
Congenital central hypoventilation
0.700
GeneticVariation
UNIPROT
An official ATS clinical policy statement: Congenital central hypoventilation syndrome: genetic basis, diagnosis, and management.
20208042
2010
rs36119840
GDNF;GDNF-AS1
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
0.700
GeneticVariation
UNIPROT
Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient.
8896568
1996
rs36119840
GDNF;GDNF-AS1
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
0.700
GeneticVariation
UNIPROT
Pathogenesis of Hirschsprung's disease.
10917288
2000
rs36119840
GDNF;GDNF-AS1
Congenital central hypoventilation
0.700
GeneticVariation
UNIPROT
Mutations of the RET-GDNF signaling pathway in Ondine's curse.
9497256
1998
rs777451569
GDNF;GDNF-AS1
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
0.700
GeneticVariation
UNIPROT
De novo mutation of GDNF, ligand for the RET/GDNFR-alpha receptor complex, in Hirschsprung disease.
8968758
1996