Gene: SNCA ×
Source: GWASCAT ×
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: rs356219
rs356219
SNCA ; LOC105377329
1 0.776 0.240 4 89716450 intron variant G/A snv 0.54 0.900 1.000 2 2008 2019
dbSNP: rs11931074
rs11931074
SNCA ; LOC105377329
1 0.851 0.080 4 89718364 intron variant G/A;C;T snv 0.900 1.000 1 2009 2020
dbSNP: rs2736990
rs2736990
SNCA
1 0.882 0.080 4 89757390 intron variant G/A;T snv 0.860 1.000 2 2009 2018
dbSNP: rs356220
rs356220
SNCA ; LOC105377329
1 0.925 0.080 4 89720189 intron variant T/A;C snv 0.850 1.000 6 2010 2016
dbSNP: rs356203
rs356203
SNCA
1 1.000 0.040 4 89744890 intron variant C/T snv 0.54 0.800 1.000 1 2011 2019
dbSNP: rs356182
rs356182
SNCA ; LOC105377329
1 0.882 0.080 4 89704960 intron variant G/A snv 0.65 0.740 1.000 3 2014 2018
dbSNP: rs8180209
rs8180209
SNCA
1 1.000 0.040 4 89723303 intron variant A/G snv 0.24 0.700 1.000 1 2017 2017