rs1561904557, CSF1R

N. diseases: 9
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.
Abnormal saccadic eye movement
CUI: C0234649
Disease: Abnormal saccadic eye movement
1 0.851 0.160 5 150056050 missense variant GGAT/TGCC mnv 0.700 0
Apathy
CUI: C0085632
Disease: Apathy
9 0.851 0.160 5 150056050 missense variant GGAT/TGCC mnv 0.700 0
Apraxias
CUI: C0003635
Disease: Apraxias
9 0.851 0.160 5 150056050 missense variant GGAT/TGCC mnv 0.700 0
Dysarthria
CUI: C0013362
Disease: Dysarthria
54 0.851 0.160 5 150056050 missense variant GGAT/TGCC mnv 0.700 0
Gait Ataxia
CUI: C0751837
Disease: Gait Ataxia
17 0.851 0.160 5 150056050 missense variant GGAT/TGCC mnv 0.700 0
Hereditary Diffuse Leukoencephalopathy with Spheroids
CUI: C3711381
Disease: Hereditary Diffuse Leukoencephalopathy with Spheroids
44 0.851 0.160 5 150056050 missense variant GGAT/TGCC mnv 0.700 0
Leukodystrophy
CUI: C0023520
Disease: Leukodystrophy
27 0.851 0.160 5 150056050 missense variant GGAT/TGCC mnv 0.700 0
Spastic gait
CUI: C0231687
Disease: Spastic gait
9 0.851 0.160 5 150056050 missense variant GGAT/TGCC mnv 0.700 0
Tremor of hands
CUI: C0239842
Disease: Tremor of hands
7 0.851 0.160 5 150056050 missense variant GGAT/TGCC mnv 0.700 0