Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28937882
rs28937882
Entrez Id: 8074
Gene Symbol: FGF23
FGF23
CUI: C0342642
Disease:
Autosomal dominant hypophosphatemic rickets
A 0.800 CausalMutation CLINVAR
dbSNP: rs28937882
rs28937882
Entrez Id: 8074
Gene Symbol: FGF23
FGF23
CUI: C0342642
Disease:
Autosomal dominant hypophosphatemic rickets
0.800 GeneticVariation UNIPROT