{{Rsnum
|rsid = 28934002
|Gene = ATP1A2
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Chromosome=1
|position=160128767
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ATP1A2
}}{{omim
|desc=ALTERNATING HEMIPLEGIA OF CHILDHOOD
|id=182340
|rsnum=28934002
|variant=0005
}}

{{ClinVar
|rsid=28934002
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=160128767
|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.160128767C>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000702.3:c.1133C>A; 182340.0005
|CLNSIG=5
|CLNCUI=C0338488
|CLNDBN=Alternating hemiplegia of childhood
|Disease=Alternating hemiplegia of childhood
|CLNACC=RCV000013784.16
|Tags=PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0338488:104290:ORPHA2131:230466004
}}

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