Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2042329
CWC27
0.882 0.120 5 64771925 intron variant T/C;G snv 3
rs197414
DDX20
0.882 0.120 1 111766501 missense variant C/A;T snv 0.12; 4.0E-06 3
rs1203030830
EGFR
0.882 0.120 7 55155873 synonymous variant T/C snv 4.0E-06 3
rs17881656
FGFR3
0.925 0.240 4 1804404 missense variant T/A;C snv 8.0E-06; 3.3E-03 3
rs771866347
GPX1
0.882 0.120 3 49358109 missense variant G/A snv 4.1E-06 3
rs9624880
GRK3
0.882 0.120 22 25588025 intron variant C/T snv 3
rs1484761909
GSTM1 ; GSTM2
0.882 0.120 1 109688224 missense variant A/G snv 3.0E-05 3.8E-05 3
rs758057623
GSTP1
0.882 0.120 11 67584520 missense variant G/A snv 3
rs10775480
LOC105372093 ; SLC14A1
0.882 0.120 18 45737317 intron variant T/C snv 0.61 3
rs140241283
MTHFR
0.882 0.120 1 11796249 start lost A/G;T snv 4.0E-06; 4.0E-06 3
rs3219493
MUTYH
0.882 0.120 1 45330597 intron variant G/C snv 0.92 0.93 3
rs17650301
POLG2 ; MILR1
0.925 0.120 17 64483156 intron variant A/C snv 0.23 3
rs1135612
POR
0.882 0.120 7 75980359 synonymous variant A/G;T snv 0.28 3
rs2228104
POR
0.882 0.120 7 75985635 synonymous variant T/A;C snv 4.5E-06; 0.92 3
rs7431
PPP3CC
0.882 0.120 8 22540949 3 prime UTR variant G/A snv 0.56 3
rs1428779969
PXN
0.882 0.120 12 120223776 missense variant G/A snv 7.0E-06 3
rs2074647
RGS6
0.882 0.120 14 72562470 missense variant G/A snv 9.0E-02 0.10 3
rs17674580
SLC14A1 ; LOC105372093
0.882 0.120 18 45729946 5 prime UTR variant C/A;T snv 3
rs7832529
SLC20A2
0.882 0.120 8 42449295 intron variant T/C snv 0.24 3
rs11077654
SLC39A11
0.882 0.120 17 73010373 intron variant A/C snv 0.69 3
rs11871756
SLC39A11
0.882 0.120 17 72730105 intron variant C/G snv 0.11 3
rs4969054
SLC39A11
0.882 0.120 17 73016334 intron variant G/C snv 0.73 3
rs9913017
SLC39A11
0.882 0.120 17 73014881 intron variant A/C;T snv 3
rs1336331763
SULT1A1
0.882 0.120 16 28606796 missense variant G/A snv 4.0E-06 3
rs2664139
THBS1
0.882 0.120 15 39580382 upstream gene variant T/C snv 0.41 3