Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 14
rs2289263
SMAD3
0.925 0.120 15 67146869 intron variant T/G snv 0.43 3
rs10218792
KIF26B
1.000 0.040 1 245587630 intron variant T/G snv 0.26 1
rs11965969
NT5DC1 ; COL10A1
1.000 0.040 6 116131040 intron variant T/G snv 0.50 1
rs2353525
BCL9
1.000 0.040 1 147597199 intron variant T/G snv 0.34 1
rs4931462 1.000 0.040 12 31225008 TF binding site variant T/G snv 0.65 1
rs62435999
LOC101929770
1.000 0.040 6 44727536 upstream gene variant T/G snv 0.28 1
rs6766414 1.000 0.040 3 31446730 intergenic variant T/G snv 0.22 1
rs945006
DIO3
1.000 0.040 14 101562940 3 prime UTR variant T/G snv 0.20 1
rs4362
ACE
0.807 0.240 17 63496400 missense variant T/C;G snv 0.52; 1.2E-05 0.51 9
rs7135617
ORAI1
0.827 0.240 12 121631099 intron variant T/C;G snv 5
rs1940475
MMP8
1.000 0.040 11 102722517 missense variant T/C;G snv 0.54 4
rs2622873
COL11A1
0.882 0.040 1 103000497 intron variant T/C;G snv 3
rs10401670
MCEMP1
1.000 0.040 19 7677916 intron variant T/C;G snv 0.49 1
rs10795550
ITIH5
1.000 0.040 10 7562392 3 prime UTR variant T/C;G snv 0.88 1
rs1355782
CPNE4
1.000 0.040 3 131768822 intron variant T/C;G snv 1
rs798726
FAM53A
1.000 0.040 4 1683484 non coding transcript exon variant T/C;G snv 1
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs1805015
IL4R
0.683 0.520 16 27362859 missense variant T/C snv 0.16 0.22 22
rs225014
DIO2
0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 22
rs679620
MMP3
0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs2232365
FOXP3
0.716 0.480 X 49259429 intron variant T/C snv 16