{{Rsnum
|rsid = 28933400
|Gene = ATP1A2
|geno1 = (C;C)
|geno2 = (C;T)
|geno3 = (T;T)
|Orientation=plus
|ReferenceAllele=T
|MissenseAllele=C
|Chromosome=1
|position=160135510
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ATP1A2
}}{{omim
|desc=MIGRAINE, FAMILIAL HEMIPLEGIC, 2
|id=182340
|rsnum=28933400
|variant=0003
}}
{{ neighbor
| rsid = 28933401
| distance = 264
}}
{{ neighbor
| rsid = 28933398
| distance = 335
}}

{{ClinVar
|rsid=28933400
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=160135510
|CHROM=1
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050268000a05000002110100
|GENEINFO=ATP1A2:477
|GENE_NAME=ATP1A2
|GENE_ID=477
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.160135510T>C
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000702.3:c.2192T>C; 182340.0003
|CLNSIG=5
|CLNCUI=C1865322
|CLNDBN=Familial hemiplegic migraine type 2
|Disease=Familial hemiplegic migraine type 2
|CLNACC=RCV000013782.22
|Tags=PM;PMC;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1388:C1865322:602481:ORPHA569
}}

{{PMID|19199261}} [Association of the polymorphisms of sodium transport related genes with essential hypertension].

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