Variant: rs386834051 

    present in Gene: MKS1;LPO;LOC105371841
    present in Chromosome: 17
    Position on Chromosome: 58219175
    Alleles of this Variant: -/CCCGG

rs386834051 in MKS1;LPO;LOC105371841 gene and BARDET-BIEDL SYNDROME 13 PMID 16415886 2006 MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome.

rs386834051 in MKS1;LPO;LOC105371841 gene and JOUBERT SYNDROME 28 PMID 16415886 2006 MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome.

rs386834051 in MKS1;LPO;LOC105371841 gene and Meckel syndrome type 1 PMID 16415886 2006 MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome.