Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs121913409
CTNNB1
0.708 0.400 3 41224646 missense variant C/A;G;T snv 21
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs10795668
LOC105376400
0.724 0.160 10 8659256 upstream gene variant G/A snv 0.24 17
rs121913228
CTNNB1
0.742 0.200 3 41224621 missense variant T/C;G snv 14
rs3789243
ABCB1
0.776 0.120 7 87591570 intron variant A/G snv 0.50 14
rs4925386
LAMA5
0.776 0.080 20 62345988 intron variant T/C snv 0.56 14
rs1060503115
PMS2
0.763 0.400 7 5978664 missense variant T/A;G snv 13
rs11255841 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 11
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins 11
rs7873784
TLR4
0.752 0.440 9 117716658 3 prime UTR variant G/A;C;T snv 11