{{Rsnum
|rsid=387907239
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HOXB1
|position=48529834
|Gene_s=HOXB1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=17
|CLNACC=RCV000029225.24
|CLNALLE=1
|CLNDBN=Facial paresis, hereditary congenital, 3
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN130589:614744:306530
|CLNHGVS=NC_000017.10:g.46607196G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=142968.0001
|Disease=Facial paresis
|FwdALT=T
|FwdREF=C
|REF=G
|RSPOS=46607196
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907239
|GENEINFO=HOXB1:3211
|GENE_ID=3211
|GENE_NAME=HOXB1
}}