{{Rsnum
|rsid=121434500
|Chromosome=20
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SNTA1
|position=33410203
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SNTA1
}}{{omim
|id=601017
|rsnum=121434500
|variant=0001
}}{{ClinVar
|rsid=121434500
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=31998009
|CHROM=20
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SNTA1:6640
|GENE_NAME=SNTA1
|GENE_ID=6640
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.31998009G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601017.0001
|CLNSIG=5
|CLNCUI=C2751830
|CLNDBN=Long QT syndrome 12
|Disease=Long QT syndrome 12
|CLNACC=RCV000008997.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1129:C2751830:612955:101016
}}