Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs28934574
TP53
0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 31
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs762551
CYP1A2
0.701 0.400 15 74749576 intron variant C/A snv 0.67 23
rs5751876
ADORA2A ; ADORA2A-AS1 ; SPECC1L-ADORA2A
0.742 0.320 22 24441333 synonymous variant T/C snv 0.54 0.52 16
rs3798577
ESR1
0.742 0.320 6 152099995 3 prime UTR variant T/C snv 0.45 16
rs2470890
CYP1A2
0.742 0.320 15 74755085 synonymous variant T/C snv 0.57 12
rs2298383
ADORA2A-AS1 ; ADORA2A ; SPECC1L-ADORA2A
0.827 0.200 22 24429543 non coding transcript exon variant C/A;T snv 11
rs5030732
UCHL1 ; UCHL1-AS1
0.790 0.160 4 41257616 missense variant C/A snv 0.24 0.16 10
rs1495741 0.827 0.240 8 18415371 regulatory region variant G/A snv 0.71 9
rs2069514 0.807 0.160 15 74745879 upstream gene variant G/A snv 0.13 9
rs2472297 0.882 0.160 15 74735539 intergenic variant C/T snv 0.16 9
rs4410790
LOC101927609 ; AHR
0.882 0.160 7 17244953 intron variant T/C snv 0.54 9
rs33949390
LRRK2
0.776 0.160 12 40320043 missense variant G/A;C;T snv 1.6E-04; 1.9E-03; 8.0E-06 9
rs73598374
ADA
0.790 0.280 20 44651586 missense variant C/A;G;T snv 7.1E-06; 6.2E-02 8
rs2470893
CYP1A1
0.882 0.160 15 74727108 upstream gene variant C/T snv 0.20 8
rs794728708
RYR2
0.827 0.120 1 237377386 missense variant G/A;T snv 8
rs1255998
ESR2
0.827 0.200 14 64227153 3 prime UTR variant G/C;T snv 6
rs118192162
RYR1
0.851 0.120 19 38455359 missense variant A/C;G snv 6
rs118192170
RYR1
0.882 0.120 19 38584989 missense variant T/A;C snv 6
rs118192177
RYR1
0.851 0.160 19 38496283 missense variant C/G;T snv 2.0E-05 6
rs118192161
RYR1
0.882 0.120 19 38444211 missense variant C/T snv 5
rs118192172
RYR1
0.851 0.120 19 38457545 missense variant C/G;T snv 8.7E-05 1.1E-04 5
rs121918600
RYR2
0.882 0.080 1 237791441 missense variant C/T snv 5