Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs115482041
rs115482041
RCL1
0.010 GeneticVariation BEFREE Despite being twice as rare (MAF<0.5%), c.1114C>T showed similar effect and significant association with depressive symptoms in samples from the independent population-based Rotterdam study (N=1604, β<sub>T-allele</sub>=3.60, P-value=3 × 10<sup>-2</sup>). 28322274

2018