{{Rsnum
|rsid=104893905
|Chromosome=5
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NKX2-5
|position=173232898
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NKX2-5
}}{{omim
|id=600584
|rsnum=104893905
|variant=0007
}}{{ClinVar
|rsid=104893905
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=172659901
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=NKX2-5:1482
|GENE_NAME=NKX2-5
|GENE_ID=1482
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.172659901G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600584.0007
|CLNSIG=5
|CLNCUI=C0039685
|CLNDBN=Tetralogy of Fallot
|Disease=Tetralogy of Fallot
|CLNACC=RCV000009575.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0039685:187500:3303:86299006
}}