Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs3212227
IL12B
0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs1057519932
PIK3CA
0.683 0.320 3 179234298 missense variant T/G snv 22
rs1057520003
TP53
0.695 0.320 17 7675996 missense variant T/G snv 20
rs6869366
XRCC4 ; TMEM167A
0.701 0.280 5 83075927 intron variant T/G snv 9.2E-02 18
rs2243115
IL12A-AS1 ; IL12A
0.776 0.320 3 159988493 intron variant T/G snv 0.10 12
rs989902
PTPN13
0.742 0.240 4 86785353 missense variant T/G snv 0.42 0.53 12
rs2228059
LOC107984200 ; IL15RA
0.882 0.080 10 5960405 missense variant T/G snv 0.51 0.55 5
rs315919
IL1RN
0.851 0.120 2 113118636 intron variant T/G snv 0.55 5
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 21
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 19
rs753660142
TP53
0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs121913228
CTNNB1
0.742 0.200 3 41224621 missense variant T/C;G snv 14
rs1035142
FLACC1
0.807 0.200 2 201288355 3 prime UTR variant T/C;G snv 0.54 7
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs1051740
EPHX1
0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs758272654
GNAS
0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs153109
IL27
0.623 0.600 16 28507775 intron variant T/C snv 0.43 37