Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519695
NRAS
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs1057519834
NRAS
0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs10484561 0.827 0.160 6 32697643 intergenic variant T/G snv 0.13 6
rs764562217
TP53
0.882 0.120 17 7673308 stop lost T/G snv 2.3E-05 3.5E-05 3
rs10462020
PER3
0.925 0.160 1 7820623 missense variant T/G snv 0.17 0.16 2
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 19
rs730882026
TP53
0.742 0.440 17 7674256 missense variant T/C;G snv 15
rs16978630
TNPO2
0.925 0.160 19 12702869 missense variant T/C;G snv 4.1E-02 2
rs2272990
RIPK1
1.000 0.120 6 3076907 missense variant T/C;G snv 0.91 1
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs1346044
WRN
0.708 0.440 8 31167138 missense variant T/C snv 0.24 0.23 23
rs3758391
SIRT1
0.742 0.480 10 67883584 upstream gene variant T/C snv 0.64 11
rs1801018
BCL2
0.851 0.240 18 63318646 synonymous variant T/C snv 0.37 0.32 6
rs11045879
SLCO1B1
1.000 0.120 12 21229685 intron variant T/C snv 0.18 4
rs2425752
NCOA5
0.851 0.160 20 46073481 intron variant T/C snv 0.79 4
rs3890745
MMEL1
0.925 0.200 1 2622185 intron variant T/C snv 0.40 4
rs751837
CDC42BPB
0.882 0.120 14 103018488 intron variant T/C snv 0.23 4
rs1227230819
GDNF ; GDNF-AS1
0.925 0.120 5 37815877 missense variant T/C snv 4.0E-06 2
rs1426981647
CHEK2
0.925 0.200 22 28710038 missense variant T/C snv 4.0E-06 2