{{Rsnum
|rsid=137852725
|Chromosome=9
|position=137814479
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=EHMT1
|Gene_s=EHMT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=plus
}}{{ClinVar
|ALT=T
|CHROM=9
|CLNALLE=1
|CLNDBN=Chromosome 9q deletion syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK47079:C0795833:610253:261494
|CLNHGVS=NC_000009.11:g.140708931C>T
|CLNSIG=5
|Disease=Chromosome 9q deletion syndrome
|FwdALT=T
|FwdREF=C
|GENEINFO=EHMT1:79813
|GENE_ID=79813
|GENE_NAME=EHMT1
|REF=C
|RSPOS=140708931
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050360000000000002110100
|WGT=0
|dbSNPBuildID=133
|rsid=137852725
|CLNACC=RCV000055966.1
|CLNSRC=GeneReviews
|CLNSRCID=NBK47079
}}