Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
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
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 15
rs1179251
IL22 ; LOC105369818
0.763 0.320 12 68251271 intron variant C/G snv 0.18 14
rs12778366
SIRT1
0.724 0.480 10 67883321 upstream gene variant T/C;G snv 13
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs603965
CCND1
0.732 0.440 11 69648142 splice region variant G/A snv 13