Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1039049
rs1039049
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
G 0.700 GeneticVariation GWASCAT Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. 26252872

2015

dbSNP: rs1041536
rs1041536
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
T 0.700 GeneticVariation GWASCAT Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. 26252872

2015

dbSNP: rs111231532
rs111231532
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
C 0.700 GeneticVariation GWASCAT Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. 26252872

2015

dbSNP: rs111600634
rs111600634
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
T 0.700 GeneticVariation GWASCAT Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. 26252872

2015

dbSNP: rs112961612
rs112961612
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
T 0.700 GeneticVariation GWASCAT Analysis of pleiotropic genetic effects on cognitive impairment, systemic inflammation, and plasma lipids in the Health and Retirement Study. 31201950

2019

dbSNP: rs113793030
rs113793030
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
T 0.700 GeneticVariation GWASCAT Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. 26252872

2015

dbSNP: rs115199861
rs115199861
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
C 0.700 GeneticVariation GWASCAT Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. 26252872

2015

dbSNP: rs115700680
rs115700680
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
T 0.700 GeneticVariation GWASCAT Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. 26252872

2015

dbSNP: rs115764752
rs115764752
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
T 0.700 GeneticVariation GWASCAT Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. 26252872

2015

dbSNP: rs116065238
rs116065238
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
A 0.700 GeneticVariation GWASCAT Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. 26252872

2015

dbSNP: rs116237496
rs116237496
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
T 0.700 GeneticVariation GWASCAT Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. 26252872

2015

dbSNP: rs11637611
rs11637611
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
C 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple novel loci associated with disease progression in subjects with mild cognitive impairment. 22833209

2011

dbSNP: rs117070989
rs117070989
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
C 0.700 GeneticVariation GWASCAT Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. 26252872

2015

dbSNP: rs117224174
rs117224174
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
G 0.700 GeneticVariation GWASCAT Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. 26252872

2015

dbSNP: rs117529438
rs117529438
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
C 0.700 GeneticVariation GWASCAT Analysis of pleiotropic genetic effects on cognitive impairment, systemic inflammation, and plasma lipids in the Health and Retirement Study. 31201950

2019

dbSNP: rs117605016
rs117605016
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
C 0.700 GeneticVariation GWASCAT Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. 26252872

2015

dbSNP: rs117932393
rs117932393
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
C 0.700 GeneticVariation GWASCAT Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. 26252872

2015

dbSNP: rs12230170
rs12230170
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
T 0.700 GeneticVariation GWASCAT Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. 26252872

2015

dbSNP: rs12435940
rs12435940
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
A 0.700 GeneticVariation GWASCAT Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. 26252872

2015

dbSNP: rs12468965
rs12468965
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
G 0.700 GeneticVariation GWASCAT Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. 26252872

2015

dbSNP: rs12624302
rs12624302
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
T 0.700 GeneticVariation GWASCAT Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. 26252872

2015

dbSNP: rs12628463
rs12628463
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
C 0.700 GeneticVariation GWASCAT Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. 26252872

2015

dbSNP: rs12752888
rs12752888
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
C 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple novel loci associated with disease progression in subjects with mild cognitive impairment. 22833209

2011

dbSNP: rs13447287
rs13447287
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
T 0.700 GeneticVariation GWASCAT Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. 26252872

2015

dbSNP: rs138901640
rs138901640
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
A 0.700 GeneticVariation GWASCAT Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. 26252872

2015