{{Rsnum
|rsid=121913656
|Chromosome=22
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MYH9
|position=36295526
|Gene_s=MYH9
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=160775
|rsnum=121913656
|variant=0007
}}{{ClinVar
|rsid=121913656
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=36691572
|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.36691572G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=160775.0007
|CLNSIG=5
|CLNCUI=C0340978; C0403445
|CLNDBN=May-Hegglin anomaly; Fechtner syndrome
|Disease=May-Hegglin anomaly; Fechtner syndrome
|CLNACC=RCV000015124.24; RCV000015125.20
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM; GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK2689:C0340978:155100; NBK2689:C0403445:153640:236422008
}}