{{Rsnum
|rsid=121908105
|Chromosome=18
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MYO5B
|position=49936289
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MYO5B
}}{{omim
|id=606540
|rsnum=121908105
|variant=0005
}}{{ClinVar
|rsid=121908105
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=47462659
|CHROM=18
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MYO5B:4645
|GENE_NAME=MYO5B
|GENE_ID=4645
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000018.9:g.47462659G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606540.0005
|CLNSIG=5
|CLNCUI=C0341306
|CLNDBN=Congenital microvillous atrophy
|Disease=Congenital microvillous atrophy
|CLNACC=RCV000004473.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0341306:251850:2290:235729009
}}