{{Rsnum
|rsid=137852726
|Chromosome=9
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=EHMT1
|position=137814468
|Gene_s=EHMT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=607001
|variant=0003
|rsnum=137852726
}}{{ClinVar
|rsid=137852726
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=140708920
|CHROM=9
|dbSNPBuildID=133
|SSR=0
|SAO=0
|VP=0x050360000000000002110100
|GENEINFO=EHMT1:79813
|GENE_NAME=EHMT1
|GENE_ID=79813
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.140708920G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK47079; 607001.0003
|CLNSIG=5
|CLNCUI=C0795833
|CLNDBN=Chromosome 9q deletion syndrome
|Disease=Chromosome 9q deletion syndrome
|CLNACC=RCV000003791.2
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK47079:C0795833:610253:261494
}}