{{Rsnum
|rsid=137852684
|Chromosome=5
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=NKX2-5
|position=173233189
|Gene_s=NKX2-5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600584
|variant=0015
|rsnum=137852684
}}{{ClinVar
|rsid=137852684
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=172660192
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000040002110100
|GENEINFO=NKX2-5:1482
|GENE_NAME=NKX2-5
|GENE_ID=1482
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.172660192C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600584.0015
|CLNSIG=5
|CLNCUI=C2673630
|CLNDBN=Hypothyroidism, congenital, nongoitrous, 5
|Disease=Hypothyroidism
|CLNACC=RCV000009584.1
|Tags=RV;PM;VLD;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2673630:225250:95712
}}