rs4884357, TARDBP

N. diseases: 6
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 0.807 0.120 1 11022301 missense variant G/A;T snv 4.0E-06 0.800 1.000 19 2008 2017
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
485 0.807 0.120 1 11022301 missense variant G/A;T snv 4.0E-06 0.020 1.000 2 2018 2018
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.807 0.120 1 11022301 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2014 2014
Childhood Neuroblastoma
CUI: C4086165
Disease: Childhood Neuroblastoma
231 0.807 0.120 1 11022301 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2014 2014
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.807 0.120 1 11022301 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2018 2018
Neuroblastoma
CUI: C0027819
Disease: Neuroblastoma
386 0.807 0.120 1 11022301 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2014 2014