{{Rsnum
|rsid=137852685
|Chromosome=5
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=NKX2-5
|position=173233062
|Gene_s=NKX2-5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600584
|variant=0016
|rsnum=137852685
}}{{ClinVar
|rsid=137852685
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=172660065
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=NKX2-5:1482
|GENE_NAME=NKX2-5
|GENE_ID=1482
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.172660065C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600584.0016
|CLNSIG=5
|CLNCUI=C2673630
|CLNDBN=Hypothyroidism, congenital, nongoitrous, 5
|Disease=Hypothyroidism
|CLNACC=RCV000009585.3
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2673630:225250:95712
}}