{{Rsnum
|rsid=137853333
|Chromosome=10
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KCNMA1
|position=77090433
|Gene_s=KCNMA1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600150
|variant=0001
|rsnum=137853333
}}{{ClinVar
|rsid=137853333
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=78850191
|CHROM=10
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=KCNMA1:3778
|GENE_NAME=KCNMA1
|GENE_ID=3778
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.78850191T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600150.0001
|CLNSIG=5
|CLNCUI=C1836173
|CLNDBN=Generalized epilepsy and paroxysmal dyskinesia
|Disease=Generalized epilepsy and paroxysmal dyskinesia
|CLNACC=RCV000010034.3
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1836173:609446:79137
}}