Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61495246
rs61495246
CYP2R1
0.010 GeneticVariation BEFREE The L99P mutation had previously been reported as a homozygous defect in an unrelated child of Nigerian origin with rickets. 27473561

2017