Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1186902
rs1186902
Entrez Id: 2569
Gene Symbol: GABRR1
GABRR1
CUI: C0149931
Disease:
Migraine Disorders
0.010 GeneticVariation BEFREE The most common polymorphisms in the GABRR genes seemed to be not associated with the risk for migraine in Caucasian Spanish people, although one of them (GABRR1 rs1186902) shows a statistically significant association with the age of onset of migraine. 28699326 2017
dbSNP: rs1186902
rs1186902
Entrez Id: 2569
Gene Symbol: GABRR1
GABRR1
CUI: C0270736
Disease:
Essential Tremor
0.010 GeneticVariation BEFREE To investigate the possible association between the GABA receptor subtype rho1, rho2, and rho3 (GABRR1, GABRR2, and GABRR3) genotypes and allelic variants of the single nucleotide polymorphisms GABRR1-M26V (Met26Val, rs12200969), GABRR1-H27R (His26Arg, rs1186902), GABRR2-T455M (Thr55Met, rs282129), and GABRR3-Y205X (Tyr205X, rs832032), and the risk for ET, we studied the frequency of the previously mentioned GABRR genotypes and allelic variants in 200 patients with ET and 250 healthy controls using TaqMan genotyping. 20820800 2011
dbSNP: rs12200969
rs12200969
Entrez Id: 2569
Gene Symbol: GABRR1
GABRR1
CUI: C0270736
Disease:
Essential Tremor
0.010 GeneticVariation BEFREE To investigate the possible association between the GABA receptor subtype rho1, rho2, and rho3 (GABRR1, GABRR2, and GABRR3) genotypes and allelic variants of the single nucleotide polymorphisms GABRR1-M26V (Met26Val, rs12200969), GABRR1-H27R (His26Arg, rs1186902), GABRR2-T455M (Thr55Met, rs282129), and GABRR3-Y205X (Tyr205X, rs832032), and the risk for ET, we studied the frequency of the previously mentioned GABRR genotypes and allelic variants in 200 patients with ET and 250 healthy controls using TaqMan genotyping. 20820800 2011
dbSNP: rs146603794
rs146603794
Entrez Id: 2569
Gene Symbol: GABRR1
GABRR1
CUI: C0270736
Disease:
Essential Tremor
0.010 GeneticVariation BEFREE To investigate the possible association between the GABA receptor subtype rho1, rho2, and rho3 (GABRR1, GABRR2, and GABRR3) genotypes and allelic variants of the single nucleotide polymorphisms GABRR1-M26V (Met26Val, rs12200969), GABRR1-H27R (His26Arg, rs1186902), GABRR2-T455M (Thr55Met, rs282129), and GABRR3-Y205X (Tyr205X, rs832032), and the risk for ET, we studied the frequency of the previously mentioned GABRR genotypes and allelic variants in 200 patients with ET and 250 healthy controls using TaqMan genotyping. 20820800 2011