rs367543041, TARDBP

N. diseases: 15
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.
AMYOTROPHIC LATERAL SCLEROSIS 10 (disorder)
CUI: C2677565
Disease: AMYOTROPHIC LATERAL SCLEROSIS 10 (disorder)
25 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 0.800 1.000 13 2008 2012
FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED
CUI: C3148872
Disease: FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED
3 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 0.700 0
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
485 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 0.090 1.000 9 2009 2016
Extrapyramidal sign
CUI: C0234133
Disease: Extrapyramidal sign
7 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 0.020 1.000 2 2011 2013
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 0.020 1.000 2 2011 2013
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 0.010 1.000 1 2014 2014
Childhood Neuroblastoma
CUI: C4086165
Disease: Childhood Neuroblastoma
231 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 0.010 1.000 1 2014 2014
Dementia
CUI: C0497327
Disease: Dementia
176 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 0.010 1.000 1 2010 2010
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 0.010 1.000 1 2011 2011
Inflammatory disorder
CUI: C1290884
Disease: Inflammatory disorder
8 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 0.010 1.000 1 2013 2013
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 0.010 1 2015 2015
Neuroblastoma
CUI: C0027819
Disease: Neuroblastoma
386 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 0.010 1.000 1 2014 2014
Neurologic Symptoms
CUI: C0235031
Disease: Neurologic Symptoms
30 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 0.010 1.000 1 2012 2012
Parkinsonian Disorders
CUI: C0242422
Disease: Parkinsonian Disorders
95 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 0.010 1.000 1 2013 2013
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 0.010 1.000 1 2010 2010