rs762060740, GFAP

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
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
485 0.827 0.080 17 44915083 missense variant G/C snv 4.0E-06 0.100 1.000 11 2005 2014
Motor Neuron Disease
CUI: C0085084
Disease: Motor Neuron Disease
52 0.827 0.080 17 44915083 missense variant G/C snv 4.0E-06 0.030 1.000 3 1996 2005
Motor neuron atrophy
CUI: C4024896
Disease: Motor neuron atrophy
21 0.827 0.080 17 44915083 missense variant G/C snv 4.0E-06 0.020 1.000 2 2008 2011
Amyotrophic Lateral Sclerosis, Familial
CUI: C4551993
Disease: Amyotrophic Lateral Sclerosis, Familial
68 0.827 0.080 17 44915083 missense variant G/C snv 4.0E-06 0.010 1.000 1 1996 1996
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.827 0.080 17 44915083 missense variant G/C snv 4.0E-06 0.010 1.000 1 2007 2007
Herpes Simplex Infections
CUI: C0019348
Disease: Herpes Simplex Infections
11 0.827 0.080 17 44915083 missense variant G/C snv 4.0E-06 0.010 1.000 1 2008 2008