Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs70991108
MSH3 ; DHFR
0.807 0.280 5 80654344 intron variant -/TCGCGCGTCCCGCCCAGGT;TGGCGCGTCCCGCCCAGGT ins 0.51 6
rs3783553
IL1A
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs712
KRAS
0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 18
rs6457327 0.790 0.320 6 31106253 downstream gene variant A/C snv 0.66 7
rs12500426
PDLIM5
0.851 0.240 4 94593458 intron variant A/C snv 0.54 5
rs2231231
AQP3
0.851 0.240 9 33442988 non coding transcript exon variant A/C snv 0.67 0.69 5
rs7201
MMP2
0.925 0.160 16 55505702 3 prime UTR variant A/C snv 0.37 4
rs770251749
MLIP
1.000 0.120 6 54121506 missense variant A/C snv 4.0E-06 2
rs1536826
CYP2E1
1.000 0.120 10 133543735 intron variant A/C snv 0.62 1
rs9260484
HLA-A
1.000 0.120 6 29952476 upstream gene variant A/C snv 0.62 1
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs11249433
EMBP1
0.827 0.160 1 121538815 intron variant A/C;G snv 9
rs2735839 0.827 0.160 19 50861367 upstream gene variant A/C;G snv 7
rs29230
GABBR1
0.807 0.440 6 29608616 missense variant A/C;G snv 4.1E-06; 0.18 6
rs3790844
NR5A2
0.882 0.200 1 200038304 intron variant A/C;G snv 4
rs7127900 0.882 0.160 11 2212344 intergenic variant A/C;G snv 3
rs7130881
LOC105369367
0.882 0.160 11 69228491 intergenic variant A/C;G snv 3
rs2076483
GABBR1
0.925 0.240 6 29603768 intron variant A/C;G snv 3.1E-05; 0.13 2
rs9110
LTF
0.851 0.200 3 46439310 missense variant A/C;G;T snv 0.39 0.40 4
rs2860580
HLA-A
1.000 0.120 6 29938914 upstream gene variant A/C;G;T snv 2
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs9138
SPP1
0.776 0.360 4 87983190 3 prime UTR variant A/C;T snv 12