Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1042636
rs1042636
CASR
CUI: C0042870
Disease: Vitamin D Deficiency
Vitamin D Deficiency 		0.010 GeneticVariation BEFREE Patients with VDD bearing the GG genotype of R990G SNPs are prone to have higher iPTH levels and lower calcium. 25695075

2015