{{Rsnum
|rsid=137852715
|Chromosome=9
|Orientation=plus
|geno1=(-;-)
|geno2=(-;GGCACCAGGAGAC)
|geno3=(GGCACCAGGAGAC;GGCACCAGGAGAC)
|Gene=EHMT1
|position=137757923
|Gene_s=EHMT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=607001
|variant=0002
|rsnum=137852715
}}{{ClinVar
|rsid=137852715
|Reversed=0
|FwdREF=GGCACCAGGAGAC
|FwdALT=
|REF=CGGCACCAGGAGAC
|ALT=C
|RSPOS=140652374
|CHROM=9
|dbSNPBuildID=133
|SSR=0
|SAO=0
|VP=0x050160000000000002110200
|GENEINFO=EHMT1:79813
|GENE_NAME=EHMT1
|GENE_ID=79813
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.140652375_140652387delGGCACCAGGAGAC
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK47079; 607001.0002
|CLNSIG=5
|CLNCUI=C0795833
|CLNDBN=Chromosome 9q deletion syndrome
|Disease=Chromosome 9q deletion syndrome
|CLNACC=RCV000003790.2
|Tags=PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK47079:C0795833:610253:261494
}}