{{Rsnum
|rsid=121918616
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ATP1A2
|position=160130283
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ATP1A2
}}{{omim
|id=182340
|rsnum=121918616
|variant=0010
}}{{ClinVar
|rsid=121918616
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=160130283
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=ATP1A2:477
|GENE_NAME=ATP1A2
|GENE_ID=477
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.160130283G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNACC=RCV000013789.16
|CLNDBN=Migraine, familial basilar
|CLNDSDB=MedGen
|CLNDSDBID=C1865323
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_000702.3:c.1643G>A; 182340.0010
|Disease=Migraine
}}