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: C0948008
Disease:
Ischemic stroke
0.010 GeneticVariation BEFREE Six main haplotypes among the rs1051006, rs326214, rs326217, rs3736101, and rs7120118 SNPs were detected in our study population, the haplotypes of G-G-T-G-C and G-A-T-G-T were associated with an increased risk of CHD and IS, respectively. 27070640 2016