Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7120118
rs7120118
Entrez Id: 10062
Gene Symbol: NR1H3
NR1H3
CUI: C0002395
Disease:
Alzheimer's Disease
0.020 GeneticVariation BEFREE Although the severity of AD did not affect NR1H3 expression, the mRNA levels of NR1H3 among the patients with CT genotype of rs7120118 were significantly increased as compared to the patients with TT genotype. 24278306 2013
dbSNP: rs7120118
rs7120118
Entrez Id: 10062
Gene Symbol: NR1H3
NR1H3
CUI: C0002395
Disease:
Alzheimer's Disease
0.020 GeneticVariation BEFREE Association analysis of the liver X receptor α (NR1H3) gene SNPs showed a protective effect for C allele carriers of rs7120118 (OR = 0.70, 95% CI 0.53-0.93), while the total-tau and phospho-tau levels in CSF were decreased in AD patients carrying the C allele. 22027013 2012