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 1.000 4 2006 2018
dbSNP: rs121913377
rs121913377
BRAF
480 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.040 1.000 4 2013 2019
dbSNP: rs397515323
rs397515323
PDK3
7 0.851 0.080 X 24503479 missense variant G/A snv 0.020 1.000 2 2013 2016
dbSNP: rs4291
rs4291
ACE
20 0.724 0.400 17 63476833 upstream gene variant T/A;C snv 0.020 1.000 2 2006 2012
dbSNP: rs63751438
rs63751438
MAPT
16 0.776 0.120 17 46010388 missense variant C/T snv 0.020 1.000 2 2010 2016
dbSNP: rs104893878
rs104893878
SNCA ; SNCA-AS1
21 0.732 0.160 4 89835580 missense variant C/G snv 0.010 1.000 1 2011 2011
dbSNP: rs1057518011
rs1057518011
TMEM240
4 1 1535766 missense variant C/T snv 0.010 1.000 1 2019 2019
dbSNP: rs1057519475
rs1057519475
FOXC1
2 1.000 0.080 6 1610761 stop gained C/T snv 0.010 1.000 1 2015 2015
dbSNP: rs1057519866
rs1057519866
NT5C2
5 0.851 0.120 10 103093198 missense variant C/T snv 0.010 1.000 1 2015 2015
dbSNP: rs1060504185
rs1060504185
CDKN2A
1 9 21971116 missense variant G/A;C snv 0.010 1.000 1 2011 2011
dbSNP: rs10938397
rs10938397 		19 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 0.010 1.000 1 2013 2013
dbSNP: rs1170695
rs1170695
SLC6A1 ; SLC6A1-AS1
2 1.000 0.040 3 11013652 5 prime UTR variant A/G snv 0.35 0.010 1.000 1 2017 2017
dbSNP: rs121908153
rs121908153
NLRP3
4 0.882 0.080 1 247424356 missense variant G/A;C snv 0.010 1.000 1 2014 2014
dbSNP: rs121908672
rs121908672
LRP5
3 0.925 0.080 11 68357802 missense variant C/T snv 0.010 1.000 1 2017 2017
dbSNP: rs121912436
rs121912436
SOD1
7 0.827 0.080 21 31667274 missense variant G/A;C snv 0.010 1.000 1 2014 2014
dbSNP: rs121912678
rs121912678
ACVR1
8 0.851 0.080 2 157774114 missense variant C/G;T snv 0.010 1.000 1 2012 2012
dbSNP: rs121913470
rs121913470
ERBB2
13 0.776 0.200 17 39723967 missense variant T/C;G snv 0.010 1.000 1 2019 2019
dbSNP: rs121918626
rs121918626
SCN1A ; SCN1A-AS1 ; LOC102724058
3 0.925 0.080 2 166012179 missense variant T/G snv 0.010 1.000 1 2020 2020
dbSNP: rs12765063
rs12765063
CREM ; CUL2
2 10 35127641 intron variant G/A snv 0.14 0.010 1.000 1 2018 2018
dbSNP: rs1331851285
rs1331851285
CASP1
2 1.000 0.080 11 105029220 missense variant T/C snv 1.4E-05 0.010 1.000 1 2014 2014
dbSNP: rs1365502141
rs1365502141
APP
1 21 26000017 missense variant G/A snv 7.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs1481318368
rs1481318368
TH
10 0.827 0.120 11 2169802 missense variant C/T snv 0.010 1.000 1 2018 2018
dbSNP: rs1541665
rs1541665
KCNIP1
2 1.000 0.040 5 170715913 intron variant C/G;T snv 0.21 0.010 1.000 1 2017 2017
dbSNP: rs1799732
rs1799732
DRD2 ; LOC105369501
11 0.790 0.160 11 113475529 intron variant -/G delins 0.010 1.000 1 2014 2014
dbSNP: rs1800544
rs1800544
ADRA2A
12 0.790 0.160 10 111076745 upstream gene variant G/C snv 0.59 0.010 1.000 1 2010 2010