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: rs104893877
rs104893877
SNCA
59 0.614 0.360 4 89828149 missense variant C/T snv 0.040 0.750 4 1998 2018
dbSNP: rs356182
rs356182
SNCA ; LOC105377329
3 0.882 0.080 4 89704960 intron variant G/A snv 0.65 0.020 1.000 2 2017 2018
dbSNP: rs10516846
rs10516846
SNCA
1 1.000 0.080 4 89775184 intron variant A/G snv 3.9E-02 0.010 1.000 1 2016 2016
dbSNP: rs356165
rs356165
SNCA
3 0.882 0.080 4 89725735 3 prime UTR variant G/A snv 0.54 0.010 < 0.001 1 2012 2012
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