Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 11
rs1343151
IL23R
0.752 0.400 1 67253446 intron variant G/A snv 0.41 10
rs1417938
CRP
0.776 0.320 1 159714396 intron variant T/A;C snv 0.28 10
rs143101792
CRP
0.851 0.320 1 159714026 stop gained G/C snv 8.8E-05 1.3E-04 5
rs3790567
IL12RB2
0.851 0.240 1 67356694 intron variant A/G snv 0.61 4
rs3218625
PTGS2
0.925 0.240 1 186674409 missense variant C/T snv 1.6E-03 5.0E-04 2
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs6430612 1.000 0.160 2 136248628 intergenic variant C/T snv 0.44 1
rs2073498
RASSF1
0.763 0.280 3 50332115 missense variant C/A snv 9.6E-02 8.0E-02 12
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs3733197
BANK1
0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs2227284
IL4
0.732 0.480 5 132677033 intron variant T/C;G snv 12
rs128738
P4HA2
0.925 0.160 5 132205182 intron variant G/T snv 0.18 2
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105