Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7799039
LOC105375494
0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs779795819
MLH1
0.925 0.080 3 37048526 frameshift variant -/ATTG delins 4.0E-06 2
rs779066883
MIR3188 ; JUND
0.925 0.080 19 18281184 missense variant G/A snv 6.2E-06 2
rs777980327
APC
0.716 0.280 5 112837567 missense variant A/T snv 4.0E-06 7.0E-06 21
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv 16
rs774904310
CDKN2A
0.925 0.080 9 21971055 frameshift variant C/- delins 3
rs7747909
IL17A
0.790 0.320 6 52189451 3 prime UTR variant G/A snv 0.18 7
rs773442580
EGF
0.851 0.080 4 109913367 missense variant T/C;G snv 4.0E-06 7
rs77191406
TNFAIP3
0.790 0.280 6 137881704 3 prime UTR variant C/T snv 7.2E-04 12
rs7656411
TLR2
0.790 0.320 4 153706503 downstream gene variant T/G snv 0.35 8
rs764986276
SHMT1
0.925 0.080 17 18333172 missense variant C/G;T snv 4.0E-06; 4.4E-05 2
rs762100304
PMS2
0.925 0.080 7 5987005 missense variant C/A;T snv 2
rs760891242
XPC
0.925 0.080 3 14168309 missense variant G/C snv 4.0E-06 7.0E-06 3
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs757128066
RIN1
0.925 0.080 11 66334745 missense variant C/A;T snv 6.9E-06; 5.5E-05 2
rs756363791
OGG1
0.882 0.080 3 9756823 missense variant G/A snv 2.0E-05 4
rs754527029
LOC105375284 ; EGFR
0.925 0.080 7 55019329 missense variant C/T snv 2
rs752021744
PIK3CB
0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs750521832
MMP8
0.732 0.200 11 102718452 missense variant A/G snv 4.0E-06 14
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs730881834
MUTYH
0.882 0.120 1 45332181 missense variant G/C snv 3
rs730881756
MSH2
0.925 0.080 2 47445653 missense variant A/C;G snv 4.0E-06 2
rs719725 0.827 0.080 9 6365683 intergenic variant A/C snv 0.34 7
rs712
KRAS
0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62