Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1429412356
rs1429412356
MAPT
0.010 GeneticVariation BEFREE Sequencing of <i>APP</i> in familial early-onset AD identified missense mutations that cause AD, while a recently discovered coding variant, APP A673T, reduces the risk for AD. 28003277

2017