{{Rsnum
|rsid=386834051
|Chromosome=17
|Orientation=minus
|geno1=(-;-)
|geno2=(-;CCGGG)
|geno3=(CCGGG;CCGGG)
|Gene=MKS1
|position=58219175
|Gene_s=MKS1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=TCCCGG
|CHROM=17
|CLNACC=RCV000050038.1
|CLNALLE=1
|CLNDBN=Meckel syndrome type 1
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN077329:249000:564
|CLNHGVS=NC_000017.10:g.56296537_56296541dupCCCGG
|CLNSIG=4
|Disease=Meckel syndrome type 1
|FwdALT=CCGGG
|REF=T
|RSPOS=56296536
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=386834051
|GENEINFO=MKS1:54903
|GENE_ID=54903
|GENE_NAME=MKS1
}}{{PMID Auto
|PMID=16415886
|Title=MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome.
}}