{{Rsnum
|rsid=121913655
|Chromosome=22
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=MYH9
|position=36348958
|Gene_s=MYH9
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=160775
|rsnum=121913655
|variant=0004
}}{{ClinVar
|rsid=121913655
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=36745003
|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.36745003G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=160775.0004
|CLNSIG=5
|CLNCUI=C0340978
|CLNDBN=May-Hegglin anomaly
|Disease=May-Hegglin anomaly
|CLNACC=RCV000015122.20
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK2689:C0340978:155100
}}