{{Rsnum
|rsid=121918619
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ATP1A2
|position=160123228
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ATP1A2
}}{{omim
|id=182340
|rsnum=121918619
|variant=0013
}}{{ClinVar
|rsid=121918619
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=160123228
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000a05040002110100
|GENEINFO=ATP1A2:477
|GENE_NAME=ATP1A2
|GENE_ID=477
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.160123228C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000702.3:c.193C>T; 182340.0013
|CLNSIG=5
|CLNCUI=C1865322
|CLNDBN=Familial hemiplegic migraine type 2
|Disease=Familial hemiplegic migraine type 2
|CLNACC=RCV000013792.21
|Tags=PM;S3D;NSM;REF;ASP;VLD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1388:C1865322:602481:ORPHA569
}}