rs104893877, SNCA

N. diseases: 59
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.
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.614 0.360 4 89828149 missense variant C/T snv 0.100 1.000 13 2000 2018
Lewy Body Variant of Alzheimer Disease
CUI: C1851958
Disease: Lewy Body Variant of Alzheimer Disease
2 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2000 2000
Parkinson Disease, Familial, Type 1
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
27 0.614 0.360 4 89828149 missense variant C/T snv 0.070 1.000 7 1998 2018
Lewy Body Disease
CUI: C0752347
Disease: Lewy Body Disease
41 0.614 0.360 4 89828149 missense variant C/T snv 0.760 1.000 6 1998 2010
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.614 0.360 4 89828149 missense variant C/T snv 0.040 0.750 4 1998 2018
Autosomal Dominant Parkinsonism
CUI: C0752098
Disease: Autosomal Dominant Parkinsonism
3 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 1998 1998
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.614 0.360 4 89828149 missense variant C/T snv 0.100 0.980 153 1997 2020
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)
CUI: C1868595
Disease: PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)
5 0.614 0.360 4 89828149 missense variant C/T snv 0.800 1.000 7 1997 2015
Young onset Parkinson disease
CUI: C4275179
Disease: Young onset Parkinson disease
32 0.614 0.360 4 89828149 missense variant C/T snv 0.040 0.750 4 1997 2002