{{Rsnum
|rsid=121912642
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LHX4
|position=180266393
|Gene_s=LHX4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=602146
|rsnum=121912642
|variant=0003
}}{{ClinVar
|rsid=121912642
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=180266393
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=LHX4:89884
|GENE_NAME=LHX4
|GENE_ID=89884
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.180266393C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_033343.3:c.250C>T; 602146.0003
|CLNSIG=5
|CLNCUI=C2678408
|CLNDBN=Pituitary hormone deficiency, combined 4
|Disease=Pituitary hormone deficiency
|CLNACC=RCV000007937.1
|Tags=PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2678408:262700:ORPHA85442
}}