Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs5361
SELE ; C1orf112
0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs1273593548
PIK3CG
0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs1537373
CDKN2B-AS1
0.925 0.120 9 22103342 intron variant T/G snv 0.63 3
rs9363918 0.882 0.200 6 68432116 intron variant T/G snv 0.38 3
rs10500715
SBF2
0.925 0.120 11 9951515 intron variant T/G snv 0.39 2
rs80358451
BRCA2
0.925 0.160 13 32333140 missense variant T/G snv 5.6E-05 6.3E-05 2
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 34
rs1800440
CYP1B1
0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 29
rs145733073
UGT1A8 ; UGT1A9 ; UGT1A7 ; UGT1A10
0.925 0.120 2 233682175 missense variant T/C;G snv 4.0E-06; 1.4E-04 2
rs199474357
HLA-A
0.925 0.120 6 29942790 missense variant T/C;G snv 2
rs1153294
BACH1
1.000 0.120 21 29328775 intron variant T/C;G snv 1
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs17107315
SPINK1
0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 40
rs34612342
MUTYH
0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 32
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs11943456
TMEM165
0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs17024869
NPAS2
0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25 10
rs1057519921
NFE2L2
0.763 0.240 2 177234231 missense variant T/C snv 10
rs372883
BACH1
0.827 0.360 21 29345416 3 prime UTR variant T/C snv 0.53 5
rs786203926
ATM
0.882 0.120 11 108227678 synonymous variant T/C snv 4