{{Rsnum
|rsid=104894269
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PHOX2A
|position=72243790
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PHOX2A
}}{{omim
|id=602753
|rsnum=104894269
|variant=0003
}}{{ClinVar
|rsid=104894269
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=71954834
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=PHOX2A:401
|GENE_NAME=PHOX2A
|GENE_ID=401
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.71954834G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602753.0003
|CLNSIG=5
|CLNCUI=C1865915
|CLNDBN=Fibrosis of extraocular muscles, congenital, 2
|Disease=Fibrosis of extraocular muscles
|CLNACC=RCV000007242.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1348:C1865915:602078
}}