{{Rsnum
|rsid = 28933401
|Gene = ATP1A2
|geno1 = (A;A)
|geno2 = (A;G)
|geno3 = (G;G)
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|Chromosome=1
|position=160135246
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ATP1A2
}}{{omim
|desc=MIGRAINE, FAMILIAL HEMIPLEGIC, 2
|id=182340
|rsnum=28933401
|variant=0004
}}
{{ neighbor
| rsid = 28933400
| distance = 264
}}

{{ClinVar
|rsid=28933401
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=160135246
|CHROM=1
|dbSNPBuildID=131
|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.160135246G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000702.3:c.2066G>A; 182340.0004
|CLNSIG=5
|CLNCUI=C1865322
|CLNDBN=Familial hemiplegic migraine type 2
|Disease=Familial hemiplegic migraine type 2
|CLNACC=RCV000013783.16
|Tags=PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1388:C1865322:602481:ORPHA569
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}