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: rs1386483
rs1386483
TPH2
9 0.790 0.080 12 72018714 intron variant T/C snv 0.53 0.010 1.000 1 2007 2007
dbSNP: rs1386494
rs1386494
TPH2
7 0.790 0.120 12 71958763 intron variant T/C;G snv 0.82 0.010 1.000 1 2007 2007
dbSNP: rs397507444
rs397507444
MTHFR
306 0.405 0.880 1 11794407 missense variant T/G snv 0.010 1.000 1 2007 2007
dbSNP: rs72554080
rs72554080
GIGYF2
3 0.925 0.040 2 232747740 missense variant A/G snv 2.6E-04 3.2E-04 0.010 1.000 1 2009 2009
dbSNP: rs9347683
rs9347683
PRKN ; PACRG
3 0.882 0.120 6 162728023 5 prime UTR variant A/C;G snv 0.020 1.000 2 2007 2011
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 2011 2011
dbSNP: rs144863268
rs144863268
SLC11A2
1 1.000 12 50992234 missense variant G/T snv 2.2E-03 1.9E-03 0.010 1.000 1 2011 2011
dbSNP: rs12678719
rs12678719
ZFPM2
2 1.000 8 105503826 intron variant C/G snv 0.37 0.010 1.000 1 2012 2012
dbSNP: rs797906
rs797906
GLIS1
2 0.925 0.040 1 53725022 intron variant C/A;T snv 0.41 0.010 1.000 1 2012 2012
dbSNP: rs112176450
rs112176450
EIF4G1
7 0.807 0.080 3 184327401 missense variant G/A;T snv 2.1E-04 2.8E-04 0.010 1.000 1 2013 2013
dbSNP: rs763222239
rs763222239
EIF4G1
5 0.827 0.040 3 184322862 missense variant G/A snv 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs1375532403
rs1375532403
CARD8
2 0.925 0.040 19 48230930 missense variant C/T snv 7.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs2072374
rs2072374
NCAPD2
1 1.000 12 6528679 splice region variant T/C snv 0.74 0.79 0.010 1.000 1 2014 2014
dbSNP: rs387907571
rs387907571
DNAJC13
6 0.827 0.080 3 132477995 missense variant A/G snv 4.2E-06 3.5E-05 0.800 1.000 1 2014 2014
dbSNP: rs7311174
rs7311174
NCAPD2
1 1.000 12 6526401 intron variant A/T snv 0.75 0.79 0.010 1.000 1 2014 2014
dbSNP: rs188286943
rs188286943
VPS35
9 0.776 0.160 16 46662452 missense variant C/T snv 0.040 1.000 4 2011 2015
dbSNP: rs145242123
rs145242123
DNAJC13
1 1.000 3 132522838 missense variant C/A;T snv 4.1E-06; 1.5E-03 0.700 1.000 2 2014 2015
dbSNP: rs146930051
rs146930051
DNAJC13
1 1.000 3 132467269 missense variant G/T snv 2.0E-05 4.2E-05 0.700 1.000 2 2014 2015
dbSNP: rs4680
rs4680
COMT ; MIR4761
249 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 0.020 1.000 2 2014 2015
dbSNP: rs4986791
rs4986791
TLR4
182 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.010 1.000 1 2015 2015
dbSNP: rs62063857
rs62063857
MAPT ; STH
3 0.882 0.120 17 45999299 missense variant A/G snv 0.14 0.15 0.010 1.000 1 2015 2015
dbSNP: rs33939927
rs33939927
LRRK2
24 0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 0.710 1.000 2 2007 2016
dbSNP: rs1130214
rs1130214
AKT1
12 0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 0.010 1.000 1 2016 2016
dbSNP: rs2230288
rs2230288
GBA
18 0.776 0.160 1 155236376 missense variant C/T snv 1.0E-02 1.0E-02 0.010 1.000 1 2016 2016
dbSNP: rs2242446
rs2242446
SLC6A2
9 0.776 0.080 16 55656513 5 prime UTR variant C/A;T snv 0.010 1.000 1 2016 2016