Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs781230344
RIMS2
1.000 0.080 8 104014559 missense variant C/G snv 4.8E-05 2
rs7356
RPA2
1.000 0.080 1 27891589 3 prime UTR variant T/A;C snv 2
rs2269349
RPSA ; SNORA62
0.925 0.080 3 39411566 non coding transcript exon variant C/T snv 0.49 2
rs2619112
ALOX15
0.882 0.160 17 4632090 intron variant A/C;G snv 4.0E-06; 0.53 3
rs1801673
ATM
0.882 0.120 11 108304736 missense variant A/T snv 4.9E-03 4.4E-03 3
rs322351
DUSP1
0.925 0.160 5 172767870 intron variant C/T snv 0.37 3
rs2632159
LOC105375751 ; PCAT1
0.882 0.080 8 127021159 intron variant G/A;T snv 3
rs2189517
RAD51B
0.882 0.080 14 68536271 intron variant A/G snv 0.49 3
rs11536898
TLR4
0.882 0.080 9 117717932 3 prime UTR variant C/A snv 0.14 3
rs750713244
EGFR
0.925 0.200 7 55157753 missense variant A/G snv 8.0E-06 4
rs3804513
IL17A
0.851 0.080 6 52188399 intron variant A/T snv 2.4E-02 4
rs17026425
IQCM
0.882 0.080 4 149751362 intron variant G/A snv 4.9E-02 4
rs462779
MFSD4B ; REV3L
0.851 0.120 6 111374684 missense variant G/A snv 0.72 0.67 4
rs1970764
PPP1R13L
0.851 0.120 19 45387615 intron variant T/C snv 0.27 4
rs11721827
TLR3
0.851 0.200 4 186069983 intron variant A/C snv 0.12 4
rs2853668 0.882 0.080 5 1299910 upstream gene variant G/T snv 0.33 5
rs776197565
APC
0.827 0.120 5 112819214 missense variant G/C;T snv 4.0E-06; 4.0E-06 5
rs10484879
IL17A
0.827 0.160 6 52187159 intron variant G/A;T snv 5
rs63750114
MLH1
0.827 0.160 3 37049015 stop gained C/A;T snv 4.9E-04 5
rs35352891
MUTYH
0.827 0.200 1 45331729 missense variant G/A snv 3.8E-04 1.1E-04 5
rs9365723
SYNJ2
0.827 0.080 6 158014540 intron variant A/C;G snv 0.56 5
rs3775292
TLR3
0.851 0.080 4 186081871 non coding transcript exon variant C/G snv 0.82 5
rs6854845 0.827 0.080 4 74821455 intergenic variant G/T snv 0.13 6
rs730881833
MUTYH
0.827 0.160 1 45332242 missense variant C/A;T snv 4.0E-06; 2.8E-05 6
rs373572
RAD18
0.882 0.120 3 8913705 missense variant C/T snv 0.68 0.70 6