{{Rsnum
|rsid=121918301
|Chromosome=9
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=EHMT1
|position=137818100
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=EHMT1
}}{{omim
|id=607001
|rsnum=121918301
|variant=0001
}}{{ClinVar
|rsid=121918301
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=140712552
|CHROM=9
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=EHMT1:79813
|GENE_NAME=EHMT1
|GENE_ID=79813
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.140712552C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK47079; 607001.0001
|CLNSIG=5
|CLNCUI=C0795833
|CLNDBN=Chromosome 9q deletion syndrome
|Disease=Chromosome 9q deletion syndrome
|CLNACC=RCV000003789.2
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK47079:C0795833:610253:261494
}}