{{Rsnum
|rsid=137852719
|Chromosome=9
|position=137777892
|Orientation=plus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=EHMT1
|Gene_s=EHMT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=CG
|CHROM=9
|CLNALLE=1
|CLNDBN=Chromosome 9q deletion syndrome
|CLNDSDB=OMIM
|CLNDSDBID=610253
|CLNHGVS=NC_000009.11:g.140672344_140672345insG
|CLNSIG=5
|Disease=Chromosome 9q deletion syndrome
|FwdALT=G
|GENEINFO=EHMT1:79813
|GENE_ID=79813
|GENE_NAME=EHMT1
|REF=C
|RSPOS=140672344
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;SLO;NSF;REF;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050160001201000002110200
|WGT=1
|dbSNPBuildID=133
|rsid=137852719
}}