Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4553808
CTLA4
0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16 28
rs747126003
IL6-AS1 ; IL6
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06 18
rs235768
BMP2
0.807 0.160 20 6778468 missense variant A/G;T snv 0.67 8
rs553668
ADRA2A
0.807 0.160 10 111079821 3 prime UTR variant A/G;T snv 8
rs10019009
DMP1 ; LOC105377323
0.851 0.080 4 87661983 missense variant A/G;T snv 4.0E-06; 0.29 4
rs7034162
NFIB
0.882 0.040 9 14190288 intron variant A/T snv 0.81 4
rs171140
ERCC2
0.807 0.080 19 45361744 non coding transcript exon variant C/A snv 0.58 0.64 6
rs2236947
RASSF1
0.882 0.040 3 50334001 intron variant C/A snv 0.39 3
rs7958904
HOTAIR
0.724 0.200 12 53963768 non coding transcript exon variant C/A;G snv 15
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs121912664
TP53
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 44
rs3212986
CD3EAP ; ERCC1
0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs764146326
TP53
0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 25
rs1799793
ERCC2
0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs28934578
TP53
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs16948627
ITGA3
0.882 0.040 17 50063432 intron variant C/A;T snv 4
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1353702185
MDM2
0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs1057519736
IDH2
0.752 0.160 15 90088605 missense variant C/G snv 13
rs3821204
IL18R1 ; IL1RL1
0.807 0.160 2 102343821 3 prime UTR variant C/G snv 0.21 6
rs2372536
ATIC
0.827 0.160 2 215325297 missense variant C/G snv 0.33 0.25 5
rs8103851
PRKCG
0.851 0.040 19 53894400 intron variant C/G snv 0.44 5