GFRA2, GDNF family receptor alpha 2, 2675

N. diseases: 27; N. variants: 10
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs15881
rs15881
Entrez Id: 2675
Gene Symbol: GFRA2
GFRA2
CUI: C2985280
Disease:
Blood Protein Measurement
C 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs15881
rs15881
Entrez Id: 2675
Gene Symbol: GFRA2
GFRA2
CUI: C2985280
Disease:
Blood Protein Measurement
C 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs36196656
rs36196656
Entrez Id: 2675
Gene Symbol: GFRA2
GFRA2
CUI: C0338451
Disease:
Frontotemporal dementia
A 0.700 GeneticVariation GWASCAT Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study. 29724592 2018
dbSNP: rs7833426
rs7833426
Entrez Id: 2675
Gene Symbol: GFRA2
GFRA2
CUI: C0005586
Disease:
Bipolar Disorder
A 0.700 GeneticVariation GWASCAT Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study. 26806518 2016
dbSNP: rs1128397
rs1128397
Entrez Id: 2675
Gene Symbol: GFRA2
GFRA2
CUI: C0036341
Disease:
Schizophrenia
0.010 GeneticVariation BEFREE On the other hand, GFRA2 variants were not associated with schizophrenia diagnosis but subjects carrying T-G-G rs1128397-rs13250096-rs4567028 haplotype were more likely to respond to clozapine treatment. 20116071 2010
dbSNP: rs13250096
rs13250096
Entrez Id: 2675
Gene Symbol: GFRA2
GFRA2
CUI: C0036341
Disease:
Schizophrenia
0.010 GeneticVariation BEFREE On the other hand, GFRA2 variants were not associated with schizophrenia diagnosis but subjects carrying T-G-G rs1128397-rs13250096-rs4567028 haplotype were more likely to respond to clozapine treatment. 20116071 2010
dbSNP: rs4567028
rs4567028
Entrez Id: 2675
Gene Symbol: GFRA2
GFRA2
CUI: C0036341
Disease:
Schizophrenia
0.010 GeneticVariation BEFREE On the other hand, GFRA2 variants were not associated with schizophrenia diagnosis but subjects carrying T-G-G rs1128397-rs13250096-rs4567028 haplotype were more likely to respond to clozapine treatment. 20116071 2010
dbSNP: rs4739217
rs4739217
Entrez Id: 2675
Gene Symbol: GFRA2
GFRA2
CUI: C3714760
Disease:
Drug-induced tardive dyskinesia
0.010 GeneticVariation BEFREE Haplotype results indicate that the minor allele of the rs4739217 is a risk factor for TD (permuted allelic p = 0.074). 20369355 2010
dbSNP: rs4739217
rs4739217
Entrez Id: 2675
Gene Symbol: GFRA2
GFRA2
CUI: C0686347
Disease:
Tardive Dyskinesia
0.010 GeneticVariation BEFREE Haplotype results indicate that the minor allele of the rs4739217 is a risk factor for TD (permuted allelic p = 0.074). 20369355 2010
dbSNP: rs6587002
rs6587002
Entrez Id: 2675
Gene Symbol: GFRA2
GFRA2
CUI: C3714760
Disease:
Drug-induced tardive dyskinesia
0.010 GeneticVariation BEFREE Moreover, carriers of the major alleles for both rs6587002 and rs4739217 presented significantly higher risk for TD (OR = 2.04, permuted p = 0.014), while subjects with the minor allele for rs4739217 and the major allele for rs6988470 were less likely to have TD (OR = 0.21, permuted p = 0.0007). 20369355 2010
dbSNP: rs6587002
rs6587002
Entrez Id: 2675
Gene Symbol: GFRA2
GFRA2
CUI: C0686347
Disease:
Tardive Dyskinesia
0.010 GeneticVariation BEFREE Moreover, carriers of the major alleles for both rs6587002 and rs4739217 presented significantly higher risk for TD (OR = 2.04, permuted p = 0.014), while subjects with the minor allele for rs4739217 and the major allele for rs6988470 were less likely to have TD (OR = 0.21, permuted p = 0.0007). 20369355 2010
dbSNP: rs6988470
rs6988470
Entrez Id: 2675
Gene Symbol: GFRA2
GFRA2
CUI: C0686347
Disease:
Tardive Dyskinesia
0.010 GeneticVariation BEFREE Moreover, carriers of the major alleles for both rs6587002 and rs4739217 presented significantly higher risk for TD (OR = 2.04, permuted p = 0.014), while subjects with the minor allele for rs4739217 and the major allele for rs6988470 were less likely to have TD (OR = 0.21, permuted p = 0.0007). 20369355 2010
dbSNP: rs6988470
rs6988470
Entrez Id: 2675
Gene Symbol: GFRA2
GFRA2
CUI: C3714760
Disease:
Drug-induced tardive dyskinesia
0.010 GeneticVariation BEFREE Moreover, carriers of the major alleles for both rs6587002 and rs4739217 presented significantly higher risk for TD (OR = 2.04, permuted p = 0.014), while subjects with the minor allele for rs4739217 and the major allele for rs6988470 were less likely to have TD (OR = 0.21, permuted p = 0.0007). 20369355 2010
dbSNP: rs1490900384
rs1490900384
Entrez Id: 2675
Gene Symbol: GFRA2
GFRA2
CUI: C1833929
Disease:
THYROID CARCINOMA, SPORADIC MEDULLARY
0.010 GeneticVariation BEFREE Recently, we described two possible low penetrance susceptibility alleles in the gene encoding RET coreceptor GFRalpha1, -193C > G and 537T > C, in a German series of sMTC. 12490080 2002