Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553763618
rs1553763618
POLR3GL
A 0.700 GeneticVariation CLINVAR

dbSNP: rs782661984
rs782661984
POLR3GL
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1159208891
rs1159208891
GALNT3
0.010 GeneticVariation BEFREE The R438H substitution likely abrogates GALNT3 activity, in turn causing enhanced FGF23 degradation and subsequent hyperostosis/hyperphosphataemia. 18322299

2008