Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7867155
LOC158435 ; ERCC6L2
0.925 0.080 9 96065532 intron variant C/T snv 0.13 2
rs75614054
PTCH1
1.000 0.040 9 95513507 intron variant C/T snv 6.7E-02 1
rs17532098
FAM120A
1.000 0.040 9 93500443 intron variant C/T snv 7.5E-02 1
rs7023933
FAM120A
1.000 0.040 9 93463196 intron variant A/T snv 0.29 1
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs10005233
SNCA
1.000 0.040 4 89822180 3 prime UTR variant C/T snv 0.58 0.59 1
rs356200
SNCA
0.882 0.160 4 89747463 intron variant T/C snv 0.44 4
rs356219
LOC105377329 ; SNCA
0.776 0.240 4 89716450 intron variant G/A snv 0.54 9
rs1555462347
USP7
0.716 0.520 16 8901028 frameshift variant CT/- delins 34
rs13328187
LINC00461
1.000 0.040 5 88569547 intron variant T/A;C snv 1
rs2194027
LINC00461
1.000 0.040 5 88526854 intron variant T/A snv 0.37 1
rs12188167
TMEM161B-AS1
1.000 0.040 5 88370488 intron variant C/G snv 0.15 1
rs2180619
CNR1
1.000 0.040 6 88168233 upstream gene variant G/A snv 0.53 3
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs7766029 0.851 0.080 6 88137716 downstream gene variant T/C snv 0.51 7
rs16902946 1.000 0.040 5 87982999 intron variant T/C snv 0.22 1
rs121909231
PTEN
0.667 0.600 10 87961095 stop gained C/A;T snv 32
rs1085308056
PTEN
0.851 0.160 10 87957850 splice region variant C/G snv 8
rs1085308045
PTEN
0.807 0.160 10 87933128 missense variant C/G;T snv 8
rs786204858
PTEN
0.776 0.280 10 87933079 missense variant A/G;T snv 11
rs587776667
PTEN
0.742 0.280 10 87931090 splice donor variant G/A;C;T snv 14
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs2254298
CAV3 ; OXTR
0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs1202184
ABCB1
0.851 0.120 7 87584585 intron variant C/T snv 0.39 7
rs1922242
ABCB1
0.827 0.120 7 87544351 intron variant A/T snv 0.43 8