Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1085307993
rs1085307993
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C4023353
Disease:
Abnormality of coordination 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1085307993
rs1085307993
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C1854882
Disease:
Absent speech 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs10051667
rs10051667
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C0001973
Disease:
Alcoholic Intoxication, Chronic 		0.010 GeneticVariation BEFREE Two additional SNPs, rs10051667 (S31) and rs967771 (S32), previously associated with alcohol dependence and bipolar disorder respectively, were also analyzed. 26561861 2015
dbSNP: rs967771
rs967771
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C0001973
Disease:
Alcoholic Intoxication, Chronic 		0.010 GeneticVariation BEFREE Two additional SNPs, rs10051667 (S31) and rs967771 (S32), previously associated with alcohol dependence and bipolar disorder respectively, were also analyzed. 26561861 2015
dbSNP: rs1085307993
rs1085307993
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C0002418
Disease:
Amblyopia 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1085307993
rs1085307993
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C0003706
Disease:
Arachnodactyly 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1085307993
rs1085307993
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C0427190
Disease:
Ataxia, Truncal 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1085307993
rs1085307993
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C0004352
Disease:
Autistic Disorder 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs10051667
rs10051667
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C0005586
Disease:
Bipolar Disorder 		0.010 GeneticVariation BEFREE Two additional SNPs, rs10051667 (S31) and rs967771 (S32), previously associated with alcohol dependence and bipolar disorder respectively, were also analyzed. 26561861 2015
dbSNP: rs967771
rs967771
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C0005586
Disease:
Bipolar Disorder 		0.010 GeneticVariation BEFREE Two additional SNPs, rs10051667 (S31) and rs967771 (S32), previously associated with alcohol dependence and bipolar disorder respectively, were also analyzed. 26561861 2015
dbSNP: rs187269
rs187269
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C0006012
Disease:
Borderline Personality Disorder 		0.010 GeneticVariation BEFREE Disease-control differences were significantly correlated with SNP rs187269 in BPD males for both beta(2S1) and beta(2S2) expressions, and significantly correlated with SNPs rs2546620 and rs187269 in SCZ males for beta(2S2) expression. 19763268 2009
dbSNP: rs2546620
rs2546620
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C0006012
Disease:
Borderline Personality Disorder 		0.010 GeneticVariation BEFREE Disease-control differences were significantly correlated with SNP rs187269 in BPD males for both beta(2S1) and beta(2S2) expressions, and significantly correlated with SNPs rs2546620 and rs187269 in SCZ males for beta(2S2) expression. 19763268 2009
dbSNP: rs1085307993
rs1085307993
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C0856863
Disease:
Broad-based gait 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs187269
rs187269
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C0006287
Disease:
Bronchopulmonary Dysplasia 		0.010 GeneticVariation BEFREE Disease-control differences were significantly correlated with SNP rs187269 in BPD males for both beta(2S1) and beta(2S2) expressions, and significantly correlated with SNPs rs2546620 and rs187269 in SCZ males for beta(2S2) expression. 19763268 2009
dbSNP: rs2546620
rs2546620
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C0006287
Disease:
Bronchopulmonary Dysplasia 		0.010 GeneticVariation BEFREE Disease-control differences were significantly correlated with SNP rs187269 in BPD males for both beta(2S1) and beta(2S2) expressions, and significantly correlated with SNPs rs2546620 and rs187269 in SCZ males for beta(2S2) expression. 19763268 2009
dbSNP: rs1085307993
rs1085307993
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C0240635
Disease:
Byzanthine arch palate 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1085307993
rs1085307993
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C0401149
Disease:
Chronic constipation 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1085307993
rs1085307993
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C1845847
Disease:
Coarse facial features 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1085307993
rs1085307993
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C1277241
Disease:
Delayed myelination 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1085307993
rs1085307993
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C0454644
Disease:
Delayed speech and language development 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1085307993
rs1085307993
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C0013421
Disease:
Dystonia 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1085307993
rs1085307993
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C4023077
Disease:
EEG with central focal spikes 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1085307993
rs1085307993
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C4025792
Disease:
EEG with irregular generalized spike and wave complexes 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1085307993
rs1085307993
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C0476397
Disease:
Electroretinogram abnormal 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1085307993
rs1085307993
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
CUI: C1963101
Disease:
Encephalopathy, CTCAE 3.0 		T 0.700 GeneticVariation CLINVAR