APOE, apolipoprotein E, 348

N. diseases: 1049; N. variants: 62
Disease: Impaired cognition ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs405509
rs405509 		0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		Mental Disorders 0.020 1.000 2 2016 2019
dbSNP: rs267606663
rs267606663 		0.925 0.080 19 44909021 missense variant G/A;C snv 7.3E-06
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs429358
rs429358 		0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs769449
rs769449 		0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		Mental Disorders 0.010 1.000 1 2014 2014