Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs770728618
IL17D
0.925 0.080 13 20721723 missense variant G/C;T snv 5.3E-05 3
rs767551092
XPC
0.790 0.200 3 14164838 missense variant G/A snv 4.0E-06 10
rs762846821
TP53
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs7597617
FLACC1
2 201338512 intron variant G/A snv 0.63 1
rs758272654
GNAS
0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs7582362
FLACC1
2 201311571 intron variant A/G snv 0.72 1
rs7579792
FLACC1
2 201335727 intron variant A/G snv 0.86 1
rs7578456 1.000 0.080 2 201370625 intergenic variant A/G snv 0.57 2
rs756826500
ERCC1
0.925 0.080 19 45413705 missense variant G/A snv 4.0E-06 5
rs753955
LOC105370113
0.776 0.120 13 23719720 regulatory region variant A/G snv 0.50 9
rs753724
PLCE1
0.882 0.080 10 94291660 intron variant G/A;C;T snv 4
rs753544 6 29812752 upstream gene variant C/T snv 0.27 1
rs753225272
FAT4
0.925 0.080 4 125491730 missense variant C/G;T snv 8.0E-06; 4.0E-06 3
rs752742313
PIK3CB
0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs750408412
CYP2E1
0.925 0.080 10 133538938 missense variant A/G snv 3
rs748676559
ACACA
0.925 0.080 17 37284932 missense variant C/T snv 4.0E-06 2.1E-05 3
rs747621669
CDKN2A
9 21970988 missense variant C/T snv 4.1E-06 1
rs7436
COL6A3
0.925 0.080 2 237324168 3 prime UTR variant T/A snv 0.10 3
rs738722
CHEK2
0.882 0.120 22 28734024 intron variant T/C snv 0.67 4
rs727503094
LRRC56 ; HRAS
0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 41
rs7248488
ZNF208
0.851 0.160 19 22005907 intron variant A/C snv 0.59 5
rs7206735 16 50114597 intron variant T/C snv 0.39 1
rs7022441
LOC101927234 ; TMC1
9 72521873 5 prime UTR variant G/A snv 0.53 1
rs698
ADH1C ; ADH1B
0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs6898743
GHR
0.776 0.160 5 42602390 intron variant C/G snv 0.78 9