Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6855911
SLC2A9
0.851 0.200 4 9934286 intron variant A/G snv 0.33 4
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 2
rs356200
SNCA
0.882 0.160 4 89747463 intron variant T/C snv 0.44 1
rs356219
LOC105377329 ; SNCA
0.776 0.240 4 89716450 intron variant G/A snv 0.54 1
rs16916239
CNGB3
8 86631513 intron variant A/G snv 0.16 1
rs342422
EDIL3
5 84175168 intron variant G/A;C snv 1
rs1458103 11 81336231 intron variant A/C snv 0.25 1
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 11
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 4
rs2451828
ADCY2
5 7448683 intron variant C/T snv 2.7E-02 1
rs34516333
ZFHX3
16 73114768 intron variant G/T snv 0.17 1
rs7528604
PDE4B
0.925 0.040 1 65941669 intron variant G/A snv 0.42 2
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 7
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 3
rs202085145
SUOX
1.000 0.080 12 56002720 missense variant G/T snv 1.0E-03 5.6E-04 6
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 5
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 5
rs3918242
MMP9
0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 1
rs5742905
CBS
0.701 0.360 21 43063074 missense variant A/G snv 4
rs6030245
PTPRT
20 42441919 intron variant T/C snv 0.30 1
rs11855560
RAD51
15 40732105 3 prime UTR variant T/C snv 0.49 1
rs6462203
SDK1
7 3636370 intron variant C/A;T snv 1
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 1
rs324981
NPSR1-AS1 ; NPSR1
0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 1
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 6