{{Rsnum
|rsid=281875281
|Chromosome=9
|position=14792753
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=FREM1
|Gene_s=FREM1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=minus
}}{{ClinVar
|ALT=C
|CHROM=9
|CLNACC=RCV000023743.1; RCV000059638.1
|CLNALLE=1
|CLNDBN=Marles Greenberg Persaud syndrome; not provided
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1728:C1855425:248450
|CLNHGVS=NC_000009.11:g.14792751A>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNSRCID=608944.0006; VAR_066412
|Disease=Marles Greenberg Persaud syndrome; not provided
|FwdALT=G
|FwdREF=T
|REF=A
|RSPOS=14792751
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050168000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=281875281
|GENEINFO=FREM1:158326
|GENE_ID=158326
|GENE_NAME=FREM1
}}{{PMID Auto
|PMID=21507892
|Title=Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1.
}}