Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs2279744
MDM2
0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs7656411
TLR2
0.790 0.320 4 153706503 downstream gene variant T/G snv 0.35 8
rs352144
TLR9
0.925 0.080 3 52227452 intron variant T/G snv 3.7E-02 3
rs12778366
SIRT1
0.724 0.480 10 67883321 upstream gene variant T/C;G snv 13
rs773442580
EGF
0.851 0.080 4 109913367 missense variant T/C;G snv 4.0E-06 7
rs3219145
PARP1
0.882 0.120 1 226363128 missense variant T/C;G snv 1.2E-02; 4.0E-06 4
rs587782513
PMS2
0.925 0.080 7 5992023 missense variant T/C;G snv 4.0E-06 2
rs680
IGF2 ; INS-IGF2
0.925 0.080 11 2132404 3 prime UTR variant T/C;G snv 0.78 2
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs3804099
TLR2
0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs3804100
TLR2
0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs34612342
MUTYH
0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 32
rs752021744
PIK3CB
0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 23
rs187115
CD44
0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs9651118
MTHFR
0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs352139
TLR9
0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs4779584 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 16
rs10759932
TLR4
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18 15
rs1342387
ADIPOR1
0.776 0.120 1 202945228 intron variant T/C snv 0.53 12
rs3753584
MTHFR ; CLCN6
0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14 10
rs4809960
CYP24A1
0.807 0.240 20 54169534 intron variant T/C snv 0.20 8