{{Rsnum
|rsid=121918408
|Chromosome=5
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=GLRA1
|position=151851406
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GLRA1
}}{{omim
|id=138491
|rsnum=121918408
|variant=0001
}}
{{omim
|id=138491
|rsnum=121918408
|variant=0002
}}{{ClinVar
|rsid=121918408
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=151230967
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=GLRA1:2741
|GENE_NAME=GLRA1
|GENE_ID=2741
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000005.9:g.151230967C>A; NC_000005.9:g.151230967C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1260; 138491.0001; 138491.0002
|CLNSIG=5
|CLNCUI=C1835614
|CLNDBN=Hyperekplexia hereditary
|Disease=Hyperekplexia hereditary
|CLNACC=RCV000017438.26; RCV000017439.23
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1260:C1835614:149400:3197
}}