Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs3748067
IL17A
0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02 21
rs7804372
CAV1
0.716 0.320 7 116554174 intron variant T/A snv 0.27 19
rs3807987
CAV1
0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 17
rs1179251
IL22 ; LOC105369818
0.763 0.320 12 68251271 intron variant C/G snv 0.18 14
rs1550117
DNMT3A
0.790 0.320 2 25343038 upstream gene variant A/G;T snv 11
rs10499563
STEAP1B
0.807 0.120 7 22720869 intron variant T/C snv 0.21 7
rs10983755 0.790 0.320 9 117702392 upstream gene variant G/A snv 3.2E-02 7
rs12229892
PTPN11
0.807 0.240 12 112485589 intron variant G/A snv 1.4E-02 6
rs3024496
IL10
0.827 0.200 1 206768519 3 prime UTR variant A/G snv 0.43 6
rs11536878
TLR4
0.827 0.240 9 117709275 intron variant C/A snv 9.5E-02 5
rs158572
ERCC8 ; NDUFAF2
0.851 0.120 5 60943616 intron variant G/A snv 0.63 4
rs1917799 0.851 0.120 10 49542929 upstream gene variant A/C snv 0.25 4
rs2301756
PTPN11
0.851 0.120 12 112452972 intron variant A/G snv 0.21 4
rs2709800
NOD1
0.882 0.120 7 30473155 intron variant A/C snv 0.53 4
rs718226
LOC102724907
0.882 0.120 16 50735652 intron variant A/G snv 0.36 4
rs1640827
TLR5
0.882 0.120 1 223138265 intron variant C/G;T snv 3
rs17163737
TLR5
0.882 0.120 1 223129809 intron variant G/T snv 7.2E-02 3
rs1878672
IL19 ; IL10
0.882 0.080 1 206770368 intron variant G/A;C;T snv 3
rs2015620
IL32
0.882 0.120 16 3073560 intron variant A/G;T snv 3