{{Rsnum
|rsid=80338830
|Chromosome=22
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=MYH9
|position=36295068
|Gene_s=MYH9
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80338830
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=36691114
|CHROM=22
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050160000000000002100100
|GENEINFO=MYH9:4627
|GENE_NAME=MYH9
|GENE_ID=4627
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.36691114C>A
|CLNORIGIN=0
|CLNSIG=5
|Tags=RV;PM;SLO;OTHERKG;LSD
|CLNACC=RCV000032221.1
|CLNDBN=MYH9 related disorders
|CLNDSDB=GeneReviews:MedGen
|CLNDSDBID=NBK2689:CN073381
|CLNSRC=GeneReviews
|CLNSRCID=NBK2689
|Disease=MYH9 related disorders
}}