Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4950928
CHI3L1
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 32
rs121913227
BRAF
0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs1800734
EPM2AIP1 ; MLH1
0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 24
rs3742330
DICER1
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24
rs712
KRAS
0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 23
rs121913273
PIK3CA
0.605 0.440 3 179218294 missense variant G/A;C snv 22
rs187115
CD44
0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs3748067
IL17A
0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02 21
rs2854744
IGFBP3
0.695 0.520 7 45921476 intron variant G/T snv 0.48 20
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 20
rs9651118
MTHFR
0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 19
rs4696480
TLR2
0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs13281615
CASC8 ; POU5F1B ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43 17
rs2167270
LEP
0.724 0.280 7 128241296 5 prime UTR variant G/A snv 0.37 17
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 17
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 16
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 16
rs10759932
TLR4
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18 15
rs121913495
GNAS
0.672 0.400 20 58909366 missense variant G/A;T snv 15
rs14035
RAN
0.742 0.320 12 130876696 3 prime UTR variant C/T snv 0.33 15