Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs767197560
NRG1
1.000 0.040 8 32760357 missense variant C/G snv 4.0E-06 1.4E-05 1
rs768388223
SERPINA3
1.000 0.040 14 94614795 synonymous variant C/T snv 4.0E-06 1
rs770029196
NRG1
1.000 0.040 8 32749563 missense variant C/G snv 4.0E-06 1
rs773016917
POTEM
1.000 0.040 14 18967839 synonymous variant C/G;T snv 1
rs845561
EGFR ; EGFR-AS1
1.000 0.040 7 55185015 intron variant C/T snv 0.76 1
rs1057519904
H3C11
0.742 0.080 6 27872233 missense variant T/A snv 17
rs1131691036
TP53
0.851 0.080 17 7675207 frameshift variant GCA/CC delins 8
rs8126
TNFAIP2
0.807 0.080 14 103137232 3 prime UTR variant C/T snv 0.63 8
rs149840192
EGFR
0.807 0.080 7 55154129 missense variant C/A;T snv 7
rs1389500636
EGFR
0.827 0.080 7 55156796 missense variant G/A snv 6
rs7213430
BRIP1
0.851 0.080 17 61682813 3 prime UTR variant G/A snv 0.61 6
rs1057519951
RHOA
0.882 0.080 3 49375472 missense variant C/G;T snv 4
rs1276184054
EGFR
0.851 0.080 7 55201305 missense variant G/A snv 4.0E-06 4
rs4663402
ATG16L1
0.851 0.080 2 233285017 intron variant A/T snv 5.1E-02 4
rs776375114
EGFR
0.851 0.080 7 55202577 missense variant G/A;C snv 4.0E-06; 4.0E-06 4
rs8136867
MAPK1
0.882 0.080 22 21850504 intron variant G/A snv 0.55 4
rs11599672
LOC105378438 ; PLCE1
0.925 0.080 10 93993019 regulatory region variant T/G snv 0.21 3
rs2237025
KIT
0.882 0.080 4 54675713 intron variant T/C snv 0.60 3
rs1057519905
H3C11
0.925 0.080 6 27872234 missense variant T/C snv 2
rs1360602468
KLC1 ; XRCC3
0.925 0.080 14 103698904 missense variant G/C;T snv 2
rs2280148
SOCS3
0.925 0.080 17 78358299 3 prime UTR variant T/G snv 2.5E-02 2
rs26537
AP3S1 ; ATG12
0.925 0.080 5 115841317 3 prime UTR variant T/C;G snv 2
rs754426793
EGFR-AS1 ; EGFR
0.925 0.080 7 55181395 missense variant G/A snv 1.2E-05 1.4E-05 2
rs1057519824
MET
0.807 0.120 7 116783374 missense variant T/G snv 10
rs1059234
CDKN1A
0.790 0.120 6 36685820 3 prime UTR variant C/T snv 0.15 0.13 10