Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs9904341
BIRC5
0.695 0.280 17 78214286 5 prime UTR variant G/A;C;T snv 0.38; 4.8E-06 20
rs980303898
LOC101929532 ; GCG
0.851 0.120 2 162147479 missense variant T/C snv 8.0E-06 7.0E-06 4
rs9582036
FLT1
0.776 0.280 13 28311271 intron variant C/A snv 0.59 8
rs9573163 0.925 0.120 13 73334709 regulatory region variant C/G;T snv 2
rs9564966 0.851 0.120 13 73322084 intergenic variant A/G snv 0.52 4
rs9543325 0.882 0.200 13 73342491 regulatory region variant C/G;T snv 3
rs9502893 0.827 0.120 6 1339954 intergenic variant C/G;T snv 5
rs949647240
TP73
0.925 0.120 1 3707693 missense variant C/T snv 2
rs940553638
ALDH2
0.827 0.200 12 111783222 missense variant G/A snv 1.6E-05 7.0E-06 6
rs9363918 0.882 0.200 6 68432116 intron variant T/G snv 0.38 3
rs935821839
TP73
0.925 0.120 1 3727199 missense variant A/G snv 7.0E-06 2
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs887303970
SOD3
0.776 0.280 4 24799565 missense variant C/T snv 8.8E-06 7.0E-06 10
rs879254154
PALB2
0.851 0.160 16 23621428 missense variant A/C;G snv 4
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs876661110
FBXO11 ; MSH6
0.925 0.120 2 47791093 missense variant G/A snv 2
rs876659900
PMS2
0.925 0.120 7 5982861 stop gained G/A snv 3
rs80359584
BRCA2
0.807 0.280 13 32340757 frameshift variant CTTAA/- delins 4.2E-06 1.4E-05 8
rs80358683
BRCA2
0.851 0.120 13 32338880 stop gained C/T snv 5
rs80358451
BRCA2
0.925 0.160 13 32333140 missense variant T/G snv 5.6E-05 6.3E-05 2
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs7993418
FLT1
0.925 0.120 13 28308924 synonymous variant G/A snv 0.80 0.67 2
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93