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 0.070 1.000 7 2001 2018
dbSNP: rs199473244
rs199473244
SCN5A
4 0.851 0.120 3 38557251 missense variant C/A snv 0.010 1.000 1 2014 2014
dbSNP: rs199473648
rs199473648
KCNE2 ; LOC105372791
4 1.000 0.080 21 34370507 missense variant C/T snv 2.5E-04 2.4E-04 0.010 1.000 1 2008 2008
dbSNP: rs200034939
rs200034939
SCN5A
3 0.882 0.080 3 38557248 missense variant C/A snv 3.2E-05 0.010 1.000 1 2014 2014
dbSNP: rs2200733
rs2200733 		12 0.752 0.240 4 110789013 intergenic variant C/T snv 0.18 0.010 1.000 1 2008 2008
dbSNP: rs3766871
rs3766871
RYR2
9 0.790 0.240 1 237614784 missense variant G/A;T snv 4.0E-02 0.010 1.000 1 2015 2015
dbSNP: rs542171324
rs542171324
SNCA
6 0.851 0.160 4 89828148 missense variant G/A;C snv 8.0E-06; 4.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs752981956
rs752981956
SNCA
1 1.000 0.080 4 89822349 missense variant C/T snv 1.6E-05 1.4E-05 0.010 1.000 1 2018 2018