Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11125
LGALS3
0.851 0.120 14 55145121 missense variant A/T snv 6.5E-02 5.7E-02 5
rs11134527
MIR218-2 ; SLIT3
0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs11202058
WAPL
0.882 0.080 10 86522854 non coding transcript exon variant G/A snv 0.25 3
rs1126497
EPCAM
0.716 0.200 2 47373967 missense variant T/C snv 0.51 0.58 14
rs1131445
IL16 ; STARD5
0.724 0.440 15 81309441 3 prime UTR variant T/A;C snv 16
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1136201
ERBB2
0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1141718
SOD2
0.724 0.280 6 159688224 missense variant A/G snv 15
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1143630
IL1B
0.827 0.160 2 112834078 intron variant T/A;G snv 5
rs115137622
HCG24 ; HLA-DPA3 ; LOC105375021
1.000 0.080 6 33143124 intron variant C/G snv 1
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs11543848
EGFR
0.790 0.240 7 55161562 missense variant G/A;C;T snv 7
rs11549465
HIF1A-AS3 ; HIF1A
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11549467
HIF1A ; HIF1A-AS3
0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs11568785
TGFBR1
0.882 0.080 9 99143552 intron variant A/G;T snv 7.2E-02 5
rs11568818
MMP7
0.763 0.280 11 102530930 upstream gene variant T/A;C snv 15
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs11655237
LINC00511 ; LINC00673
0.724 0.280 17 72404025 non coding transcript exon variant C/T snv 0.16 17
rs11674595
IL1R2
0.763 0.200 2 101994530 intron variant T/C snv 0.22 13
rs1179225338
TLR4
0.851 0.120 9 117713505 synonymous variant C/T snv 4.0E-06 4
rs1195571 0.882 0.080 12 130739483 intergenic variant T/C snv 0.97 3
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1207011218
CTLA4
0.742 0.440 2 203870794 synonymous variant C/T snv 12