rs121912562, NR3C2

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
0.700 CausalMutation CLINVAR Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations. 30763456 2019
Pseudohypoaldosteronism, Type I, Autosomal Dominant
CUI: C1449842
Disease: Pseudohypoaldosteronism, Type I, Autosomal Dominant
0.700 CausalMutation CLINVAR