{{Rsnum
|rsid=74315376
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TBX19
|position=168305136
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TBX19
}}{{omim
|id=604614
|rsnum=74315376
|variant=0001
}}{{ClinVar
|rsid=74315376
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=168305136
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000605000002110100
|GENEINFO=TBX19:9095
|GENE_NAME=TBX19
|GENE_ID=9095
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.168305136C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_005149.2:c.856C>T; 604614.0001
|CLNSIG=5
|CLNCUI=C0342388
|CLNDBN=ACTH deficiency
|Disease=ACTH deficiency
|CLNACC=RCV000005773.1
|Tags=PM;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1169:C0342388:201400:ORPHA199296:237692001
}}