{{Rsnum
|rsid=121909501
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TDGF1
|position=46579986
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TDGF1
}}{{omim
|id=187395
|rsnum=121909501
|variant=0001
}}{{ClinVar
|rsid=121909501
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=46621476
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=TDGF1:6997
|GENE_NAME=TDGF1
|GENE_ID=6997
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.46621476C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000013565.16
|CLNDBN=Forebrain defects
|CLNDSDB=MedGen
|CLNDSDBID=C1861235
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=187395.0001
|Disease=Forebrain defects
}}