Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs33388
rs33388
Entrez Id: 2908
Gene Symbol: NR3C1
NR3C1
CUI: C0027726
Disease:
Nephrotic Syndrome
0.010 GeneticVariation BEFREE We genotyped 118 children diagnosed with NS who initially responded to oral GC treatment [steroid-responsive nephrotic syndrome (SRNS) group] and 136 healthy children for three intron B single nucleotide polymorphisms of NR3C1, namely Bcl I (C/G), rs33389 (C/T) and rs33388 (A/T). 18343955 2008
dbSNP: rs33389
rs33389
Entrez Id: 2908
Gene Symbol: NR3C1
NR3C1
CUI: C0027726
Disease:
Nephrotic Syndrome
0.010 GeneticVariation BEFREE We genotyped 118 children diagnosed with NS who initially responded to oral GC treatment [steroid-responsive nephrotic syndrome (SRNS) group] and 136 healthy children for three intron B single nucleotide polymorphisms of NR3C1, namely Bcl I (C/G), rs33389 (C/T) and rs33388 (A/T). 18343955 2008