Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519830
EGFR
1.000 0.040 7 55163737 missense variant C/T snv 3
rs1057519887
EGFR
0.925 0.040 7 55154128 missense variant GC/AA;AT mnv 3
rs1057519888
EGFR
0.925 0.080 7 55143386 missense variant A/G snv 3
rs1203030830
EGFR
0.882 0.120 7 55155873 synonymous variant T/C snv 4.0E-06 3
rs121913418
EGFR
0.882 0.160 7 55174818 missense variant G/A;T snv 3
rs121913430
EGFR
1.000 0.080 7 55174740 missense variant G/A snv 3
rs139236063
EGFR
0.925 0.080 7 55165350 missense variant G/C;T snv 3
rs1405999227
EGFR
0.925 0.160 7 55156637 missense variant A/G snv 4.0E-06 3
rs1420841957
EGFR
0.882 0.080 7 55201275 missense variant G/C snv 4.0E-06 7.0E-06 3
rs148934350
EGFR
0.882 0.080 7 55191792 missense variant C/A;T snv 8.0E-06; 3.6E-04 3
rs150036236
EGFR
0.925 0.080 7 55191741 missense variant G/A snv 4.8E-05 3.5E-05 3
rs17172432
EGFR
0.882 0.080 7 55073624 intron variant T/C snv 0.31 3
rs556324078
EGFR
7 55205514 missense variant T/C snv 4.0E-06 3
rs727504256
EGFR
0.882 0.080 7 55173984 missense variant G/A snv 8.0E-06 3
rs757699239
EGFR
0.882 0.080 7 55201269 missense variant G/A;C snv 8.0E-06; 4.0E-06 3
rs763317
EGFR
0.882 0.080 7 55027504 intron variant A/G snv 0.59 3
rs767505234
EGFR
1.000 0.040 7 55174033 missense variant C/T snv 1.4E-05 3
rs769696078
EGFR
0.925 0.040 7 55154128 missense variant G/A snv 3
rs770443325
EGFR
0.882 0.080 7 55172994 missense variant C/G;T snv 2.8E-05 3
rs773454677
EGFR
0.925 0.160 7 55205466 missense variant G/A snv 1.2E-05 3
rs780439043
EGFR
0.925 0.080 7 55205301 missense variant A/G snv 8.0E-06 1.4E-05 3
rs781609053
EGFR
0.925 0.120 7 55200379 missense variant T/C snv 1.2E-05 3
rs867182279
EGFR
0.882 0.080 7 55205510 missense variant T/C snv 3
rs961150162
EGFR
7 55198779 missense variant G/A;C snv 3
rs13222385
EGFR-AS1 ; EGFR
1.000 0.160 7 55183900 intron variant A/G snv 0.28 3