Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10462020
PER3
0.925 0.160 1 7820623 missense variant T/G snv 0.17 0.16 2
rs10484561 0.827 0.160 6 32697643 intergenic variant T/G snv 0.13 6
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
rs1057520009
XPO1
0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 14
rs11045879
SLCO1B1
1.000 0.120 12 21229685 intron variant T/C snv 0.18 4
rs111724149
PRDM11
0.925 0.120 11 45204720 missense variant A/G snv 1.8E-03 1.8E-03 2
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs1164376164
ABCB1
0.851 0.200 7 87601024 5 prime UTR variant A/G snv 6
rs116446171 0.851 0.160 6 484453 downstream gene variant C/G snv 2.3E-02 4
rs1178732315
GBA
0.882 0.240 1 155236381 missense variant A/G snv 1.4E-05 3
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121912654
TP53
0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05 21
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs121913238
KRAS
0.732 0.240 12 25227343 missense variant G/C;T snv 17
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 25
rs121913254
NRAS
0.658 0.440 1 114713909 stop gained G/A;C;T snv 31
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480