Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 35
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 27
rs77543610
FGFR2
0.667 0.560 10 121520160 missense variant G/C snv 12
rs121913344
TP53
0.925 0.200 17 7673704 stop gained G/A;T snv 5
rs1789924
ADH1C
0.925 0.160 4 99353129 upstream gene variant C/G;T snv 4
rs121913231
EGFR
1.000 0.080 7 55174794 missense variant C/T snv 8.0E-06 2
rs971074
ADH7
0.925 0.040 4 99420704 synonymous variant C/T snv 0.12 0.13 1
rs1057519830
EGFR
1.000 0.040 7 55163737 missense variant C/T snv 1
rs146795390
EGFR
0.827 0.080 7 55191776 missense variant G/A snv 8.0E-06 7.0E-06 1
rs1494961
HELQ
0.925 0.160 4 83453327 missense variant C/T snv 0.56 0.60 1
rs4767364
NAA25
0.807 0.160 12 112083644 intron variant G/A snv 0.45 1