Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1372519
SNCA-AS1 ; SNCA
1.000 0.040 4 89836158 5 prime UTR variant A/G snv 0.77 1
rs363236
PDZD8 ; SLC18A2
1.000 0.040 10 117278860 3 prime UTR variant C/A;T snv 0.77 1
rs738499
TEF ; LOC105373042
0.851 0.120 22 41381096 intron variant G/T snv 0.76 9
rs3772715
LAMP3
1.000 0.040 3 183131776 intron variant C/T snv 0.76 1
rs6971
TSPO
0.742 0.200 22 43162920 missense variant A/G snv 0.76 0.75 11
rs2572323
SNCA ; LOC105377329
1.000 0.040 4 89713401 intron variant A/G snv 0.75 1
rs2270363
HMOX2 ; NMRAL1
0.882 0.080 16 4476291 5 prime UTR variant A/G snv 0.74 3
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs4752293
GRK5
0.882 0.080 10 119342186 intron variant C/T snv 0.74 3
rs4911414 0.882 0.120 20 34141638 regulatory region variant T/G snv 0.73 5
rs2280104
BIN3
1.000 0.040 8 22668467 intron variant T/A;C;G snv 0.73 1
rs2070676
CYP2E1
0.827 0.320 10 133537633 non coding transcript exon variant G/C snv 0.73 5
rs1014290
SLC2A9 ; LOC105374476
0.827 0.280 4 10000237 intron variant G/A snv 0.72 6
rs356169
LOC105377329 ; SNCA
1.000 0.040 4 89711617 intron variant G/T snv 0.72 1
rs356174
SNCA ; LOC105377329
1.000 0.040 4 89709750 intron variant G/T snv 0.72 1
rs8193036
IL17A
0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs165815
ARVCF
0.882 0.120 22 19971950 missense variant C/T snv 0.75 0.72 5
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1362858
LOC105372063
0.925 0.040 18 35406636 upstream gene variant C/A snv 0.71 2
rs7702187
SEMA5A
0.925 0.040 5 9332169 intron variant T/A snv 0.70 2
rs823156
SLC41A1
1.000 0.040 1 205795512 non coding transcript exon variant G/A snv 0.77 0.70 1
rs972936
IGF1 ; LINC02456
0.807 0.200 12 102431143 intron variant T/C snv 0.70 12
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs1635291
LINC02210-CRHR1
1.000 0.040 17 45674547 intron variant G/A snv 0.69 2