rs761079751, ALPL

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hypophosphatasia
CUI: C0020630
Disease: Hypophosphatasia
0.010 GeneticVariation BEFREE Identification of novel missense mutations (Phe310Leu and Gly439Arg) in a neonatal case of hypophosphatasia. 8954059 1996