{{Rsnum
|rsid=121912610
|Chromosome=9
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FREM1
|position=14784494
|Gene_s=FREM1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=608944
|rsnum=121912610
|variant=0003
}}{{ClinVar
|rsid=121912610
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=14784492
|CHROM=9
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=FREM1:158326
|GENE_NAME=FREM1
|GENE_ID=158326
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.14784492C>T
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=608944.0003; VAR_063423
|CLNSIG=5
|CLNCUI=C2750433
|CLNDBN=Bifid nose with or without anorectal and renal anomalies; not provided
|Disease=Bifid nose with or without anorectal and renal anomalies; not provided
|CLNACC=RCV000002067.1; RCV000059639.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2750433:608980:217266
}}{{PMID Auto
|PMID=19732862
|Title=FREM1 mutations cause bifid nose, renal agenesis, and anorectal malformations syndrome.
|OA=1
}}