{{Rsnum
|rsid=16996652
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Chromosome=22
|position=36300203
|Gene=MYH9
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MYH9
}}{{PMID Auto
|PMID=19891592
|Title=Association Among Polymorphisms at MYH9, Environmental Factors, and Nonsyndromic Orofacial Clefts in Western China
}}

{{ClinVar
|rsid=16996652
|Reversed=0
|FwdREF=A
|FwdALT=T
|REF=A
|ALT=T
|RSPOS=36696249
|CHROM=22
|dbSNPBuildID=123
|SSR=0
|SAO=1
|VP=0x050368000000000502100101
|GENEINFO=MYH9:4627
|GENE_NAME=MYH9
|GENE_ID=4627
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.36696249A>T
|CLNORIGIN=0
|CLNSIG=2
|Tags=PM;PMC;S3D;SLO;HD;GNO;OTHERKG;LSD
|CLNACC=RCV000032219.1
|CLNDBN=MYH9 related disorders
|CLNDSDB=GeneReviews:MedGen
|CLNDSDBID=NBK2689:CN073381
|CLNSRC=GeneReviews
|CLNSRCID=NBK2689
|Disease=MYH9 related disorders
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}