Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2059691
CHROMR ; PRKRA
0.882 0.080 2 178437157 intron variant A/G snv 0.72 3
rs2189517
RAD51B
0.882 0.080 14 68536271 intron variant A/G snv 0.49 3
rs4562
ELP5 ; CLDN7
0.925 0.080 17 7260420 missense variant A/G snv 0.65 0.70 3
rs6598964
LIN28A
0.882 0.080 1 26419836 intron variant A/G snv 0.67 3
rs7911488
MIR1307 ; ATP5MD
0.882 0.080 10 103394332 5 prime UTR variant A/G snv 0.34 0.26 3
rs4548444
MAPKAPK2
0.925 0.080 1 206716793 intron variant A/G snv 0.20 2
rs8039880
MAP2K1
0.925 0.080 15 66468004 intron variant A/G snv 0.21 2
rs9694958
IKBKB ; LOC105379395
0.925 0.080 8 42298528 intron variant A/G snv 0.26 2
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1044129
AVEN ; RYR3
0.790 0.200 15 33866065 3 prime UTR variant A/G;T snv 9
rs1425164489
TCN2
0.925 0.080 22 30617374 missense variant A/G;T snv 4.0E-06 2
rs2243828
MPO
0.925 0.080 17 58281523 upstream gene variant A/G;T snv 2
rs397517132
EGFR
0.623 0.280 7 55191846 missense variant A/T snv 48
rs777980327
APC
0.716 0.280 5 112837567 missense variant A/T snv 4.0E-06 7.0E-06 21
rs3804513
IL17A
0.851 0.080 6 52188399 intron variant A/T snv 2.4E-02 4
rs121913227
BRAF
0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs774904310
CDKN2A
0.925 0.080 9 21971055 frameshift variant C/- delins 3
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs961253 0.732 0.240 20 6423634 intergenic variant C/A snv 0.34 15
rs4803455
TGFB1
0.752 0.280 19 41345604 intron variant C/A snv 0.51 11
rs8176318
BRCA1
0.807 0.120 17 43045257 3 prime UTR variant C/A snv 0.34 0.29 6
rs11536898
TLR4
0.882 0.080 9 117717932 3 prime UTR variant C/A snv 0.14 3
rs3219489
MUTYH
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27 24