Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs58064122
GFAP
0.882 0.160 17 44913334 missense variant G/A;C snv 3
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs6089953
RTEL1-TNFRSF6B ; RTEL1
0.882 0.080 20 63659655 intron variant A/G snv 0.82 3
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs7115578
MAML2
0.882 0.040 11 96266936 intron variant G/A snv 0.37 3
rs71305152
ZFPM2
0.882 0.040 8 105437494 intron variant -/TTTTCT delins 0.43 5
rs766727892
TCF7L2
0.925 0.040 10 113151107 missense variant G/A snv 1.2E-05 7.0E-06 3
rs773442580
EGF
0.851 0.080 4 109913367 missense variant T/C;G snv 4.0E-06 7
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs866419664
TP53
0.882 0.040 17 7673821 frameshift variant -/TCCCA delins 5
rs867657798
TCF4
0.925 0.040 18 55631366 missense variant G/A;C snv 1.4E-05 3
rs868162712
TCF4
0.925 0.040 18 55279598 missense variant G/A snv 3
rs9288516
XRCC5
0.827 0.120 2 216188541 intron variant T/A snv 5.0E-02 6