Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs140241283
MTHFR
0.882 0.120 1 11796249 start lost A/G;T snv 4.0E-06; 4.0E-06 3
rs1428779969
PXN
0.882 0.120 12 120223776 missense variant G/A snv 7.0E-06 3
rs1484761909
GSTM1 ; GSTM2
0.882 0.120 1 109688224 missense variant A/G snv 3.0E-05 3.8E-05 3
rs17650301
POLG2 ; MILR1
0.925 0.120 17 64483156 intron variant A/C snv 0.23 3
rs17674580
SLC14A1 ; LOC105372093
0.882 0.120 18 45729946 5 prime UTR variant C/A;T snv 3
rs197414
DDX20
0.882 0.120 1 111766501 missense variant C/A;T snv 0.12; 4.0E-06 3
rs2042329
CWC27
0.882 0.120 5 64771925 intron variant T/C;G snv 3
rs2074647
RGS6
0.882 0.120 14 72562470 missense variant G/A snv 9.0E-02 0.10 3
rs2228104
POR
0.882 0.120 7 75985635 synonymous variant T/A;C snv 4.5E-06; 0.92 3
rs2664139
THBS1
0.882 0.120 15 39580382 upstream gene variant T/C snv 0.41 3
rs3213255
XRCC1
0.882 0.120 19 43573355 intron variant G/A snv 0.60 3
rs3213356
XRCC1
0.882 0.120 19 43554087 intron variant C/T snv 0.60 3
rs3219493
MUTYH
0.882 0.120 1 45330597 intron variant G/C snv 0.92 0.93 3
rs377062126
TXNRD1
0.882 0.120 12 104319543 missense variant G/A snv 2.1E-05 3.5E-05 3
rs4969054
SLC39A11
0.882 0.120 17 73016334 intron variant G/C snv 0.73 3
rs4986826
AHR
0.882 0.120 7 17339533 missense variant G/A snv 7.8E-03 2.2E-02 3
rs62185668 0.925 0.120 20 10981287 intron variant C/A snv 0.19 3
rs6464268 0.882 0.120 7 152684065 intergenic variant A/G snv 0.23 3
rs715021 0.882 0.120 2 221196620 intergenic variant C/G snv 0.26 3
rs72552316
TLR7
0.882 0.120 X 12889591 3 prime UTR variant T/C snv 3
rs7257330
CCNE1
0.882 0.120 19 29810916 upstream gene variant G/A snv 0.30 3
rs7431
PPP3CC
0.882 0.120 8 22540949 3 prime UTR variant G/A snv 0.56 3
rs758057623
GSTP1
0.882 0.120 11 67584520 missense variant G/A snv 3
rs771866347
GPX1
0.882 0.120 3 49358109 missense variant G/A snv 4.1E-06 3
rs7832529
SLC20A2
0.882 0.120 8 42449295 intron variant T/C snv 0.24 3