Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs139599857
XRCC1
0.882 0.120 19 43545922 missense variant C/G snv 1.6E-05 2.1E-05 3
rs139632793
OGG1
0.925 0.120 3 9751114 missense variant G/C snv 5.2E-05 1.7E-04 2
rs141095230
MGMT
0.925 0.120 10 129536277 missense variant C/A;T snv 8.0E-06; 5.2E-05 2
rs1412335442
PIK3CG
0.925 0.120 7 106868317 missense variant G/T snv 7.0E-06 2
rs1447826 1.000 0.120 3 74669607 intergenic variant T/A;C;G snv 1
rs1448106115
PMS2
0.925 0.120 7 5989944 missense variant T/C snv 4.0E-06 2
rs1455311
LINC01088
0.925 0.160 4 79043433 intron variant A/G snv 0.14 2
rs145574072
OGG1
0.925 0.120 3 9754765 synonymous variant T/C snv 4.0E-06 2
rs145733073
UGT1A8 ; UGT1A9 ; UGT1A7 ; UGT1A10
0.925 0.120 2 233682175 missense variant T/C;G snv 4.0E-06; 1.4E-04 2
rs1458766475
C1orf112 ; SELE
0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs149243735
OGG1
0.925 0.120 3 9751076 missense variant C/A snv 4.0E-06 2
rs149617956
MITF
0.672 0.560 3 69964940 missense variant G/A snv 1.4E-03 1.6E-03 32
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs150495372
ADH1B
0.925 0.120 4 99313834 missense variant C/T snv 3.7E-04 3
rs1517037 0.882 0.120 18 59211042 intergenic variant C/T snv 0.23 3
rs1537373
CDKN2B-AS1
0.925 0.120 9 22103342 intron variant T/G snv 0.63 3
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1547374
LOC105372815
0.925 0.120 21 42358786 downstream gene variant A/G snv 0.32 2
rs1552462 0.925 0.120 11 7235910 upstream gene variant C/T snv 2.7E-02 2
rs1555461176
PALB2
1.000 0.120 16 23634893 stop gained -/T delins 1
rs1555525012
TP53
0.882 0.200 17 7673603 missense variant G/A snv 3
rs1561927
LINC00824
0.807 0.280 8 128555832 intron variant C/T snv 0.65 6
rs1630747
SLC5A3 ; MRPS6
0.925 0.120 21 34085692 intron variant C/A snv 0.69 2
rs169068
SSTR5-AS1 ; SSTR5
0.742 0.280 16 1079872 missense variant C/T snv 0.54 0.50 12
rs1693482
ADH1C ; ADH1B
0.807 0.240 4 99342808 missense variant C/T snv 0.34 0.31 12