Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1040411
ATG5
1.000 0.120 6 106150148 intron variant G/A snv 0.47 3
rs10420252
COX6B1
1.000 0.080 19 35648270 upstream gene variant G/A snv 9.7E-02 2
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1047781
LOC105447645 ; FUT2
0.790 0.200 19 48703374 missense variant A/T snv 3.6E-02 1.2E-02 9
rs104894228
LRRC56 ; HRAS
0.605 0.560 11 534286 missense variant C/A;G;T snv 22
rs1049074086
CTSD
0.925 0.120 11 1759567 missense variant A/G snv 7.0E-06 9
rs10491121
LOC101927369 ; CCL4
0.882 0.120 17 36102943 upstream gene variant G/A snv 0.32 5
rs1051660
OPRK1
1.000 0.080 8 53251002 synonymous variant C/A;T snv 0.11 3
rs1052667
ARHGAP35
0.882 0.040 19 47004177 3 prime UTR variant C/G;T snv 6
rs1053129
DHFR
5 80626901 3 prime UTR variant C/A;T snv 1
rs1056123575
ADAMTS1
0.925 0.080 21 26844557 missense variant G/A snv 4.2E-06 7.0E-06 4
rs1056629
MPHOSPH6
0.827 0.120 16 82148499 3 prime UTR variant T/C snv 0.14 6
rs1057519695
NRAS
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs1057519710
KIT
0.695 0.280 4 54733166 missense variant G/C;T snv 22
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 9
rs1057519816
ERBB2
0.763 0.200 17 39711955 missense variant C/A;T snv 6
rs1057519824
MET
0.807 0.120 7 116783374 missense variant T/G snv 9
rs1057519834
NRAS
0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs1057519847
EGFR
0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs1057519864
AR
0.851 0.080 X 67723707 missense variant T/C snv 8
rs1057519874
RAC1
0.807 0.120 7 6387261 missense variant C/A;T snv 6
rs1057519902
H3-3A
0.742 0.160 1 226064451 missense variant G/C snv 13
rs1057519903
H3-3A
0.683 0.080 1 226064434 missense variant A/T snv 26
rs1057519904
H3C11
0.742 0.080 6 27872233 missense variant T/A snv 14