rs4912905, NR3C1

N. diseases: 3
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Bodily Pain
CUI: C3890602
Disease: Bodily Pain
0.010 GeneticVariation BEFREE The rs4912905 polymorphism was associated with improvement in bodily pain (P = 0.040) and general health (P = 0.038). 26255187 2015
Infantile Spasm
CUI: C3887898
Disease: Infantile Spasm
0.010 GeneticVariation BEFREE The haplotype TG of two SNPs (rs6877893 and rs4912905) was associated with a decreased risk of IS (P=0.038, OR=0.66, 95% CI=0.45-0.98), whereas haplotype TC being homozygous was associated with an increased risk of IS (P=0.015, OR=2.60, 95% CI=1.20-5.60). 22728713 2012
West Syndrome
CUI: C0037769
Disease: West Syndrome
0.010 GeneticVariation BEFREE The haplotype TG of two SNPs (rs6877893 and rs4912905) was associated with a decreased risk of IS (P=0.038, OR=0.66, 95% CI=0.45-0.98), whereas haplotype TC being homozygous was associated with an increased risk of IS (P=0.015, OR=2.60, 95% CI=1.20-5.60). 22728713 2012