Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs142293996
rs142293996
NVL
0.010 GeneticVariation BEFREE After correction for multiple testing, the C allele of rs142293996 in an intron of nuclear VCP-like (<i>NVL</i>) was associated with DR in European discovery cohorts (<i>P</i> = 2.1 × 10<sup>-9</sup>), but did not reach genome-wide significance after meta-analysis with replication cohorts. 30487263

2019