{{Rsnum
|rsid=137854504
|Chromosome=9
|Orientation=minus
|geno1=(GC;GC)
|geno2=(GC;TCCT)
|geno3=(TCCT;TCCT)
|Gene=LHX3
|position=136199844
|Gene_s=LHX3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600577
|variant=0005
|rsnum=137854504
}}{{ClinVar
|rsid=137854504
|Reversed=1
|FwdREF=GC
|FwdALT=TCCT
|REF=TGC
|ALT=TAGGA
|RSPOS=139091689
|CHROM=9
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110200
|GENEINFO=LHX3:8022
|GENE_NAME=LHX3
|GENE_ID=8022
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.139091690_139091691delGCinsAGGA
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600577.0005
|CLNSIG=5
|CLNCUI=C1857330
|CLNDBN=Pituitary hormone deficiency, combined 3
|Disease=Pituitary hormone deficiency
|CLNACC=RCV000009591.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1857330:221750:231720
}}