Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs771590775
TERT
1.000 0.040 5 1294350 missense variant C/A;G snv 1
rs765660823
DDR2
0.882 0.200 1 162778720 missense variant A/C snv 1.9E-04 4
rs764496629
RAF1
1.000 0.040 3 12590859 missense variant C/T snv 1
rs762846821
TP53
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs75790006 0.851 0.040 4 43211547 intron variant T/G snv 1.1E-02 4
rs756340448
ERCC2
0.790 0.240 19 45369135 synonymous variant G/A snv 4.0E-06 7.0E-06 8
rs754626
SRC
0.925 0.080 20 37388937 intron variant T/G snv 0.25 2
rs754332870
TP53
0.790 0.240 17 7676240 missense variant C/G snv 4.0E-06 9
rs752742313
PIK3CB
0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs751402
ERCC5 ; BIVM-ERCC5
0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs749140677
VDR
0.752 0.240 12 47857185 missense variant G/A snv 8.0E-06 13
rs74664507 1.000 0.040 9 16913838 upstream gene variant T/A snv 3
rs74653330
OCA2
0.851 0.200 15 27983407 missense variant C/T snv 8.4E-03 6.2E-03 5
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs735482
CD3EAP ; ERCC1
0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs7335046 0.807 0.040 13 99389484 downstream gene variant G/C snv 0.80 7
rs7309332 1.000 0.040 12 7938243 upstream gene variant T/C snv 0.59 3
rs7297245
HAL
0.882 0.040 12 95980836 missense variant C/T snv 0.85 0.86 4
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs7250795
ZNF763 ; ZNF69
1.000 0.040 19 11978928 missense variant C/G;T snv 4.0E-06; 1.7E-02 1
rs7242481
ELP2 ; SLC39A6
0.925 0.080 18 36129254 5 prime UTR variant G/A snv 0.35 2
rs7208422
TMC8
0.807 0.120 17 78134494 missense variant A/C;T snv 4.0E-06; 0.51 6
rs7182283
NEIL1
0.925 0.120 15 75351418 intron variant G/T snv 0.43 2
rs7097008 1.000 0.040 10 67849782 non coding transcript exon variant C/A snv 0.60 1
rs6819385
CHRNA9
0.925 0.080 4 40337557 intron variant A/G snv 0.52 2