Gene: SNCA ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10005233
rs10005233
SNCA
1 1.000 0.040 4 89822180 3 prime UTR variant C/T snv 0.58 0.59 0.700 1.000 1 2018 2018
dbSNP: rs104893877
rs104893877
SNCA
59 0.614 0.360 4 89828149 missense variant C/T snv 0.030 1.000 3 2013 2020
dbSNP: rs356200
rs356200
SNCA
4 0.882 0.160 4 89747463 intron variant T/C snv 0.44 0.010 1.000 1 2018 2018
dbSNP: rs356219
rs356219
SNCA ; LOC105377329
9 0.776 0.240 4 89716450 intron variant G/A snv 0.54 0.010 1.000 1 2018 2018