rs3173615, TMEM106B

N. diseases: 12
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.
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 0.700 1.000 1 2018 2018
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 0.700 1.000 1 2018 2018
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 0.030 1.000 3 2013 2017
DIARRHEA 5, WITH TUFTING ENTEROPATHY, CONGENITAL
CUI: C2750737
Disease: DIARRHEA 5, WITH TUFTING ENTEROPATHY, CONGENITAL
11 0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 0.020 1.000 2 2015 2018
Bradykinesia
CUI: C0233565
Disease: Bradykinesia
16 0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 0.010 1.000 1 2017 2017
Frontotemporal Lobar Degeneration
CUI: C0751072
Disease: Frontotemporal Lobar Degeneration
54 0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 0.010 1.000 1 2020 2020
Motor Neuron Disease
CUI: C0085084
Disease: Motor Neuron Disease
52 0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 0.010 1.000 1 2014 2014
Muscle Rigidity
CUI: C0026837
Disease: Muscle Rigidity
25 0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 0.010 1.000 1 2017 2017
Neurodegenerative Disorders
CUI: C0524851
Disease: Neurodegenerative Disorders
85 0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 0.010 1.000 1 2018 2018
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 0.010 1.000 1 2017 2017
Pick Disease of the Brain
CUI: C0236642
Disease: Pick Disease of the Brain
83 0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 0.010 1.000 1 2013 2013
Tremor
CUI: C0040822
Disease: Tremor
52 0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 0.010 1.000 1 2017 2017