{{Rsnum
|rsid=121909673
|Chromosome=5
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=GABRG2
|position=162093965
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GABRG2
}}{{omim
|id=137164
|rsnum=121909673
|variant=0002
}}{{ClinVar
|rsid=121909673
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=161520971
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=GABRG2:2566
|GENE_NAME=GABRG2
|GENE_ID=2566
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.161520971G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=137164.0002
|CLNSIG=255
|CLNCUI=C1843244; C1969810
|CLNDBN=Epilepsy, childhood absence 2; Familial febrile seizures 8
|Disease=Epilepsy; Familial febrile seizures 8
|CLNACC=RCV000017592.1; RCV000017593.26
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM; MedGen:OMIM:Orphanet
|CLNDSDBID=C1843244:607681; C1969810:611277:36387
}}