{{Rsnum
|rsid=137852694
|Chromosome=14
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NKX2-1
|position=36517739
|Gene_s=NKX2-1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600635
|variant=0009
|rsnum=137852694
}}{{ClinVar
|rsid=137852694
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=36986944
|CHROM=14
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=NKX2-1-AS1:100506237; NKX2-1:7080
|GENE_NAME=NKX2-1-AS1; NKX2-1
|GENE_ID=100506237; 7080
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.36986944G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600635.0009
|CLNSIG=5
|CLNCUI=C0393584
|CLNDBN=Benign hereditary chorea
|Disease=Benign hereditary chorea
|CLNACC=RCV000009543.3
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C0393584:118700:230306001
}}