rs5848, FAM171A2;GRN

N. diseases: 17
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 0.700 1.000 2 2018 2018
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 0.080 1.000 8 2009 2017
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 0.050 1.000 5 2009 2016
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 0.040 1.000 4 2008 2016
Frontotemporal Lobar Degeneration
CUI: C0751072
Disease: Frontotemporal Lobar Degeneration
54 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 0.040 0.750 4 2009 2015
GRN-related frontotemporal dementia
CUI: C3811918
Disease: GRN-related frontotemporal dementia
20 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 0.030 0.667 3 2009 2013
Hippocampal sclerosis
CUI: C1504404
Disease: Hippocampal sclerosis
14 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 0.030 1.000 3 2010 2014
Pick Disease of the Brain
CUI: C0236642
Disease: Pick Disease of the Brain
83 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 0.020 1.000 2 2008 2016
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 0.010 1.000 1 2017 2017
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
485 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 0.010 1.000 1 2015 2015
Bipolar I disorder
CUI: C0853193
Disease: Bipolar I disorder
46 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 0.010 1.000 1 2014 2014
Bipolar II disorder
CUI: C0236788
Disease: Bipolar II disorder
12 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 0.010 1.000 1 2014 2014
Dementia
CUI: C0497327
Disease: Dementia
176 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 0.010 1.000 1 2011 2011
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
23 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 0.010 1.000 1 2009 2009
Neurodegenerative Disorders
CUI: C0524851
Disease: Neurodegenerative Disorders
85 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 0.010 1.000 1 2015 2015
Posterior cortical atrophy syndrome
CUI: C4275079
Disease: Posterior cortical atrophy syndrome
8 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 0.010 1.000 1 2016 2016
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 0.010 1.000 1 2011 2011