Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11608072
rs11608072
Entrez Id: 6327
Gene Symbol: SCN2B
SCN2B
CUI: C0202236
Disease:
Triglycerides measurement
0.700 GeneticVariation GWASDB A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection. 19074352 2008