Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1405999227
EGFR
0.925 0.160 7 55156637 missense variant A/G snv 4.0E-06 3
rs121434569
EGFR-AS1 ; EGFR
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs1057519861
EGFR ; EGFR-AS1
0.776 0.080 7 55181398 missense variant T/A snv 15
rs1057519847
EGFR
0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs121434568
EGFR
0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs471979
NLRP5
0.925 0.080 19 56027610 missense variant G/C snv 0.13 9.7E-02 3
rs2640
EIF2AK1
0.925 0.080 7 6026819 missense variant T/C snv 9.0E-02 5.5E-02 3
rs483352809
TUBB4A
0.882 0.120 19 6495754 missense variant C/T snv 5
rs1057519864
AR
0.851 0.080 X 67723707 missense variant T/C snv 8
rs7201637
HSD17B2
1.000 16 82081670 intron variant T/A snv 9.0E-02 2
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs391745 0.925 0.080 X 97839482 intergenic variant C/G;T snv 3