Variant: rs104893896 

    present in Gene: MSX2
    present in Chromosome: 5
    Position on Chromosome: 174729294
    Alleles of this Variant: G/A

rs104893896 in MSX2 gene and PARIETAL FORAMINA 1 PMID 10767351 2000 Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagna.

PMID 10742103 2000 Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification.