{{Rsnum
|rsid=387906667
|Chromosome=1
|position=170719822
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PRRX1
|Gene_s=PRRX1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=1
|CLNACC=RCV000022701.24
|CLNALLE=1
|CLNDBN=Dysgnathia complex
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1530:C1876185:202650:ORPHA990
|CLNHGVS=NC_000001.11:g.170719822T>C
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_006902.4:c.338T>C; 167420.0001
|Disease=Dysgnathia complex
|FwdALT=C
|FwdREF=T
|REF=T
|RSPOS=170719822
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;NSM;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000a05000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=387906667
|GENEINFO=PRRX1:5396
|GENE_ID=5396
|GENE_NAME=PRRX1
|CLNORIGIN=1
}}