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: rs1001179
rs1001179
CAT
33 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2019 2019
dbSNP: rs10014396
rs10014396
SNCA
1 1.000 0.040 4 89791478 intron variant T/C snv 0.17 0.010 1.000 1 2012 2012
dbSNP: rs10079250
rs10079250
CSF1R
7 0.827 0.120 5 150070569 missense variant T/C snv 9.9E-02 8.6E-02 0.010 1.000 1 2019 2019
dbSNP: rs1013639215
rs1013639215
PITX3
1 1.000 0.040 10 102231987 missense variant C/G;T snv 4.1E-06 0.010 1.000 1 2010 2010
dbSNP: rs1014290
rs1014290
SLC2A9 ; LOC105374476
6 0.827 0.280 4 10000237 intron variant G/A snv 0.72 0.010 1.000 1 2017 2017
dbSNP: rs10214163
rs10214163
SV2C
1 1.000 0.040 5 75998585 intergenic variant C/A;T snv 0.010 < 0.001 1 2013 2013
dbSNP: rs1024611
rs1024611 		63 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2019 2019
dbSNP: rs10247962
rs10247962
TFR2
2 1.000 0.040 7 100622306 intron variant G/A snv 0.88 0.010 1.000 1 2014 2014
dbSNP: rs10380
rs10380
MTRR
6 0.807 0.200 5 7897078 missense variant C/T snv 0.16 0.18 0.010 1.000 1 2011 2011
dbSNP: rs10410544
rs10410544
SIRT2
6 0.827 0.120 19 38894892 intron variant T/C snv 0.68 0.67 0.010 < 0.001 1 2019 2019
dbSNP: rs1043424
rs1043424
PINK1 ; PINK1-AS
1 1.000 0.040 1 20650507 missense variant A/C snv 0.29 0.28 0.010 1.000 1 2004 2004
dbSNP: rs1044397
rs1044397
CHRNA4
7 0.851 0.160 20 63349752 synonymous variant C/T snv 0.48 0.41 0.010 1.000 1 2015 2015
dbSNP: rs1048230
rs1048230
SLC11A2
5 0.827 0.160 12 50992283 synonymous variant A/G snv 0.17 0.15 0.010 1.000 1 2015 2015
dbSNP: rs1048603
rs1048603
USP40
1 1.000 0.040 2 233485841 missense variant G/A;T snv 0.32; 1.6E-05 0.010 1.000 1 2010 2010
dbSNP: rs104893863
rs104893863
QDPR
2 0.925 0.120 4 17511987 missense variant C/T snv 1.4E-05 0.010 1.000 1 2016 2016
dbSNP: rs104894104
rs104894104
CDKN2A
7 0.790 0.160 9 21971019 missense variant G/A;T snv 0.010 1.000 1 2007 2007
dbSNP: rs1049296
rs1049296
TF
4 0.882 0.120 3 133775510 missense variant C/T snv 0.16 0.14 0.010 1.000 1 2014 2014
dbSNP: rs1049793
rs1049793
AOC1 ; LOC105375567
4 0.882 0.080 7 150860577 missense variant C/G;T snv 0.37 0.37 0.010 1.000 1 2008 2008
dbSNP: rs1051169
rs1051169
S100B
5 0.851 0.200 21 46602317 synonymous variant C/A;G;T snv 0.65 0.010 1.000 1 2018 2018
dbSNP: rs1051308
rs1051308
HMOX2 ; CDIP1
3 0.882 0.080 16 4510300 3 prime UTR variant G/A snv 0.54 0.010 1.000 1 2017 2017
dbSNP: rs1051312
rs1051312
SNAP25 ; SNAP25-AS1
5 0.827 0.120 20 10306440 3 prime UTR variant T/C snv 0.20 0.010 1.000 1 2019 2019
dbSNP: rs1051689897
rs1051689897
MBD5
1 1.000 0.040 2 148489766 synonymous variant T/C snv 8.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs1051931
rs1051931
PLA2G7
19 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 0.010 1.000 1 2005 2005
dbSNP: rs1052352
rs1052352
FUS
2 0.925 0.120 16 31183958 synonymous variant C/T snv 0.53 0.45 0.010 1.000 1 2014 2014
dbSNP: rs1057519492
rs1057519492
NLRP1
2 0.925 0.040 17 5583798 missense variant C/T snv 0.010 1.000 1 2010 2010