Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
0.020 GeneticVariation BEFREE Although functional studies are required to elucidate the role of rs73069071 in AD pathophysiology, our results support the recently growing evidence on the role of amylin in AD. 27021820 2017
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
0.020 GeneticVariation BEFREE Furthermore, both rs704180 and rs73069071 risk genotypes were associated with widespread brain atrophy visualized by MRI (Alzheimer's Disease Neuroimaging Initiative data; n = 1239). 27815632 2016
Amyloidosis
CUI: C0002726
Disease: Amyloidosis
0.010 GeneticVariation BEFREE Using postmortem beta-amyloid immunohistochemistry data from 243 AD participants in the Religious Orders Study and Memory and Aging Project, we also observed similar rs73069071-by-beta-amyloid deposition interaction effect on global cognitive function (P<sub>one-tailed</sub>=0.005). 27021820 2017
SPHEROCYTOSIS, TYPE 1 (disorder)
CUI: C2674218
Disease: SPHEROCYTOSIS, TYPE 1 (disorder)
0.010 GeneticVariation BEFREE We found that the rs73069071 risk genotype was associated with hippocampal sclerosis (HS) pathology among people with the rs704180 risk genotype (National Alzheimer's Coordinating Center/Alzheimer's Disease Genetic Consortium data; n = 2113, including 241 autopsy-confirmed HS cases). 27815632 2016
Cerebral atrophy
CUI: C0235946
Disease: Cerebral atrophy
0.010 GeneticVariation BEFREE Furthermore, both rs704180 and rs73069071 risk genotypes were associated with widespread brain atrophy visualized by MRI (Alzheimer's Disease Neuroimaging Initiative data; n = 1239). 27815632 2016
Brain atrophy
CUI: C4551584
Disease: Brain atrophy
0.010 GeneticVariation BEFREE Furthermore, both rs704180 and rs73069071 risk genotypes were associated with widespread brain atrophy visualized by MRI (Alzheimer's Disease Neuroimaging Initiative data; n = 1239). 27815632 2016
Hippocampal sclerosis
CUI: C1504404
Disease: Hippocampal sclerosis
0.010 GeneticVariation BEFREE We found that the rs73069071 risk genotype was associated with hippocampal sclerosis (HS) pathology among people with the rs704180 risk genotype (National Alzheimer's Coordinating Center/Alzheimer's Disease Genetic Consortium data; n = 2113, including 241 autopsy-confirmed HS cases). 27815632 2016