Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042602
LOC107984363 ; TYR
0.925 0.080 11 89178528 missense variant C/A snv 0.25 0.24 6
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs1047325
S100A2
1.000 0.040 1 153561551 missense variant C/T snv 7.1E-02 0.16 2
rs1047840
EXO1
0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs1048638
CA9
0.807 0.160 9 35681125 3 prime UTR variant C/A;G snv 10
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs10491121
LOC101927369 ; CCL4
0.882 0.120 17 36102943 upstream gene variant G/A snv 0.32 5
rs1050631
SLC39A6
0.882 0.080 18 36114157 synonymous variant G/A snv 0.33 0.30 4
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1057519824
MET
0.807 0.120 7 116783374 missense variant T/G snv 10
rs1057519847
EGFR
0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs1057519911
MAPK1
0.776 0.160 22 21772875 missense variant C/T snv 10
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs1057520004
TP53
0.752 0.240 17 7674884 missense variant A/C;T snv 12
rs1057520018
STK11
0.807 0.080 19 1223124 missense variant T/C snv 6
rs1057520039
STK11
0.882 0.200 19 1207169 stop gained C/G;T snv 4
rs1064793400
MLH1
1.000 0.040 3 37048550 missense variant G/A snv 1
rs1064793981
MSH2
1.000 0.040 2 47475030 missense variant G/A snv 1
rs10759637
SLC31A1 ; CDC26
1.000 0.040 9 113262744 3 prime UTR variant A/C snv 0.47 2
rs1078305
GSN
1.000 0.040 9 121289122 intron variant A/G snv 0.70 1
rs10810657 0.827 0.080 9 16884588 regulatory region variant T/A;G snv 7