{{Rsnum
|rsid=121434356
|Chromosome=13
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FREM2
|position=38784703
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FREM2
}}{{omim
|id=608945
|rsnum=121434356
|variant=0003
}}{{ClinVar
|rsid=121434356
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=39358840
|CHROM=13
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=FREM2:341640
|GENE_NAME=FREM2
|GENE_ID=341640
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.39358840G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608945.0003
|CLNSIG=5
|CLNCUI=C0265233
|CLNDBN=Cryptophthalmos syndrome
|Disease=Cryptophthalmos syndrome
|CLNACC=RCV000002064.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0265233:219000:2052:204102004
}}