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: rs10005233
rs10005233
SNCA
1 1.000 0.040 4 89822180 3 prime UTR variant C/T snv 0.58 0.59 0.700 1.000 1 2018 2018
dbSNP: rs10034259
rs10034259
LINC02503
1 1.000 0.040 4 104012596 intron variant A/C snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs1006737
rs1006737
CACNA1C
27 0.695 0.120 12 2236129 intron variant G/A snv 0.36 0.010 1.000 1 2011 2011
dbSNP: rs10112596
rs10112596
GATA4
3 0.925 0.120 8 11722293 intron variant A/G snv 0.83 0.010 1.000 1 2018 2018
dbSNP: rs1017730
rs1017730
AGBL2
1 1.000 0.040 11 47711942 intron variant G/A snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs104893877
rs104893877
SNCA
59 0.614 0.360 4 89828149 missense variant C/T snv 0.030 1.000 3 2013 2020
dbSNP: rs1048943
rs1048943
CYP1A1
88 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.010 1.000 1 2010 2010
dbSNP: rs1049353
rs1049353
CNR1
42 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 0.010 1.000 1 2008 2008
dbSNP: rs10501320
rs10501320
MADD ; MADD-AS1
5 0.925 0.120 11 47272248 5 prime UTR variant G/C snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs10507274
rs10507274
C12orf49
2 1.000 0.040 12 116723171 missense variant T/C snv 4.7E-02 4.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs1051730
rs1051730
CHRNA3
43 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 0.020 < 0.001 2 2013 2014
dbSNP: rs1057518806
rs1057518806
HMBS
4 1.000 0.040 11 119093155 frameshift variant G/- del 0.700 0
dbSNP: rs10769256
rs10769256
SPI1
1 1.000 0.040 11 47356845 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10801153
rs10801153 		3 0.925 0.080 1 192794818 intron variant G/A snv 0.27 0.010 1.000 1 2015 2015
dbSNP: rs10850379
rs10850379
MMAB
1 1.000 0.040 12 109564972 non coding transcript exon variant C/T snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs1085308045
rs1085308045
PTEN
8 0.807 0.160 10 87933128 missense variant C/G;T snv 0.700 0
dbSNP: rs1085308056
rs1085308056
PTEN
8 0.851 0.160 10 87957850 splice region variant C/G snv 0.700 0
dbSNP: rs10871777
rs10871777 		6 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs110402
rs110402
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
12 0.790 0.120 17 45802681 intron variant G/A;C snv 0.020 1.000 2 2013 2019
dbSNP: rs11090045
rs11090045
ZC3H7B
2 1.000 0.040 22 41357599 3 prime UTR variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs1110976
rs1110976
DRD2
3 1.000 0.040 11 113413797 intron variant T/G snv 0.010 1.000 1 2008 2008
dbSNP: rs11111
rs11111
GDNF ; GDNF-AS1
5 0.882 0.080 5 37814000 3 prime UTR variant T/C snv 0.22 0.010 1.000 1 2013 2013
dbSNP: rs11159097
rs11159097 		1 1.000 0.040 14 74633180 intergenic variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs11191392
rs11191392
WBP1L
1 1.000 0.040 10 102767194 intron variant C/A snv 0.49 0.700 1.000 1 2018 2018
dbSNP: rs11204421
rs11204421 		1 1.000 0.040 17 19994492 intergenic variant T/C snv 0.44 0.700 1.000 1 2018 2018