Variant: rs386834052 

    present in Gene: LPO;MKS1;LOC105371841
    present in Chromosome: 17
    Position on Chromosome: 58219149
    Alleles of this Variant: A/G

rs386834052 in LPO;MKS1;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.

rs386834052 in LPO;MKS1;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.

rs386834052 in LPO;MKS1;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.