{{Rsnum
|rsid=121913657
|Chromosome=22
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MYH9
|position=36348950
|Gene_s=MYH9
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=160775
|rsnum=121913657
|variant=0012
}}{{ClinVar
|rsid=121913657
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=36744995
|CHROM=22
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MYH9:4627
|GENE_NAME=MYH9
|GENE_ID=4627
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.36744995G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK2689; 160775.0012
|CLNSIG=5
|CLNCUI=C0398641
|CLNDBN=Epstein syndrome; MYH9 related disorders
|Disease=Epstein syndrome; MYH9 related disorders
|CLNACC=RCV000015138.20; RCV000055880.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:SNOMED_CT; GeneReviews:MedGen
|CLNDSDBID=NBK2689:C0398641:153650:234485006; NBK2689:CN073381
}}