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rs211037

From SNPedia

Orientationplus
Stabilizedplus
Make rs211037(C;C)
Make rs211037(C;T)
Make rs211037(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position162101274
GeneGABRG2
is asnp
is mentioned by
dbSNPrs211037
ebirs211037
HLIrs211037
Exacrs211037
Varsomers211037
Maprs211037
PheGenIrs211037
hapmaprs211037
1000 genomesrs211037
hgdprs211037
ensemblrs211037
gopubmedrs211037
geneviewrs211037
scholarrs211037
googlers211037
pharmgkbrs211037
gwascentralrs211037
openSNPrs211037
23andMers211037
23andMe allrs211037
SNP Nexus

SNPshotrs211037
SNPdbers211037
MSV3drs211037
GWAS Ctlgrs211037
GMAF0.3976
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 20356767] Association of alpha subunit of GABA(A) receptor subtype gene polymorphisms with epilepsy susceptibility and drug resistance in north Indian population


[PMID 22572707] Investigation of the role of the GABRG2 gene variant in migraine


[PMID 19842164OA-icon.png] Association study between GABA receptor genes and anxiety spectrum disorders.


[PMID 23140995] GABRG2 rs211037 polymorphism and epilepsy: A systematic review and meta-analysis


[PMID 23287319] Lack of association between rs211037 of the GABRG2 gene and juvenile myoclonic epilepsy in Brazilian population


[PMID 24482035] Benzodiazepine-Associated Hepatic Encephalopathy Significantly Increased Healthcare Utilization and Medical Costs of Chinese Cirrhotic Patients: 7-Year Experience


ClinVar
Risk rs211037(T;T)
Alt rs211037(T;T)
Reference rs211037(C;C)
Significance Other
Disease not specified
Variation info
Gene GABRG2
CLNDBN not specified
Reversed 0
HGVS NC_000005.9:g.161528280C>T
CLNSRC ClinVar Emory University University of Chicago
CLNACC RCV000079320.7,



[PMID 26452361] Contribution of GABRG2 Polymorphisms to Risk of Epilepsy and Febrile Seizure: a Multicenter Cohort Study and Meta-analysis