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
rs202195689
MIR4274 ; SORCS2
1.000 0.080 4 7460097 mature miRNA variant -/C;CACCC;CCC delins 1
rs712
KRAS
0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs11721827
TLR3
0.851 0.200 4 186069983 intron variant A/C snv 0.12 4
rs74790047
CHD4
0.851 0.120 12 6601978 missense variant A/C;G snv 2.0E-05; 1.2E-04; 5.2E-03 1.7E-03 7
rs9365723
SYNJ2
0.827 0.080 6 158014540 intron variant A/C;G snv 0.56 5
rs2619112
ALOX15
0.882 0.160 17 4632090 intron variant A/C;G snv 4.0E-06; 0.53 3
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs876658657
MLH1
0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs937283
MDM2
0.716 0.200 12 68808384 5 prime UTR variant A/G snv 0.37 19
rs1061624
TNFRSF1B
0.776 0.320 1 12207208 3 prime UTR variant A/G snv 0.48 8
rs1126667
ALOX12 ; ALOX12-AS1
0.776 0.280 17 6999441 missense variant A/G snv 0.60 0.62 8
rs750713244
EGFR
0.925 0.200 7 55157753 missense variant A/G snv 8.0E-06 4
rs2189517
RAD51B
0.882 0.080 14 68536271 intron variant A/G snv 0.49 3
rs1525489 1.000 0.080 7 122993419 downstream gene variant A/G snv 3.6E-02 1
rs4646903
CYP1A1
0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36
rs3804513
IL17A
0.851 0.080 6 52188399 intron variant A/T snv 2.4E-02 4
rs1801673
ATM
0.882 0.120 11 108304736 missense variant A/T snv 4.9E-03 4.4E-03 3
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs4803455
TGFB1
0.752 0.280 19 41345604 intron variant C/A snv 0.51 11