rs112176450, EIF4G1

N. diseases: 7
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.
PARKINSON DISEASE 18
CUI: C3280271
Disease: PARKINSON DISEASE 18
2 0.807 0.080 3 184327401 missense variant G/A;T snv 2.1E-04 2.8E-04 0.800 0
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.807 0.080 3 184327401 missense variant G/A;T snv 2.1E-04 2.8E-04 0.080 0.875 8 2013 2015
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.807 0.080 3 184327401 missense variant G/A;T snv 2.1E-04 2.8E-04 0.040 1.000 4 2011 2015
Lewy Body Disease
CUI: C0752347
Disease: Lewy Body Disease
41 0.807 0.080 3 184327401 missense variant G/A;T snv 2.1E-04 2.8E-04 0.010 1.000 1 2011 2011
PARKINSON DISEASE, LATE-ONSET
CUI: C3160718
Disease: PARKINSON DISEASE, LATE-ONSET
76 0.807 0.080 3 184327401 missense variant G/A;T snv 2.1E-04 2.8E-04 0.010 1.000 1 2013 2013
Parkinsonian Disorders
CUI: C0242422
Disease: Parkinsonian Disorders
95 0.807 0.080 3 184327401 missense variant G/A;T snv 2.1E-04 2.8E-04 0.010 1.000 1 2011 2011
Sporadic Parkinson disease
CUI: C4511452
Disease: Sporadic Parkinson disease
65 0.807 0.080 3 184327401 missense variant G/A;T snv 2.1E-04 2.8E-04 0.010 1 2013 2013