Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1243180
MLLT10
0.790 0.160 10 21626690 intron variant T/A snv 0.23 7
rs1265794840
ERCC2
0.851 0.160 19 45365131 missense variant C/T snv 7.0E-06 6
rs12921862
AXIN1
0.763 0.200 16 331927 intron variant C/A snv 0.18 10
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1413299
COL15A1
0.925 0.120 9 98998959 intron variant G/A;T snv 2
rs142091544 0.925 0.120 5 168286995 upstream gene variant C/T snv 2.1E-02 2
rs144848
BRCA2
0.653 0.440 13 32332592 missense variant A/C snv 0.28 0.23 29
rs1456079929
PGR
0.851 0.120 11 101042001 missense variant C/A snv 8.0E-06 5
rs146314922
NLRP2
0.925 0.120 19 54982828 missense variant A/G snv 2
rs149652370
RUVBL1
0.925 0.120 3 128084115 non coding transcript exon variant A/G snv 1.3E-04 2
rs1574560 1.000 0.120 3 166329716 intergenic variant T/C snv 0.42 1
rs1596797
MUC16
0.925 0.120 19 8977341 missense variant T/A;C;G snv 2.0E-05; 4.0E-06; 0.74 2
rs1614627 1.000 0.120 1 20620263 downstream gene variant A/C snv 0.86 1
rs1649942
NRG3
0.925 0.120 10 82191935 intron variant G/A;C snv 3
rs16917496
KMT5A
0.689 0.360 12 123409283 3 prime UTR variant C/G;T snv 21
rs16949649
NME1 ; NME1-NME2
0.776 0.200 17 51152947 upstream gene variant T/C snv 0.39 12
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs17106154
RAD51B
0.925 0.120 14 68694457 non coding transcript exon variant T/C snv 7.8E-02 2
rs17130142
PKN2-AS1
1.000 0.120 1 87773925 intron variant G/A snv 6.5E-02 1
rs17250239
TRAF2
0.925 0.120 9 136902178 non coding transcript exon variant G/A snv 7.2E-02 2
rs17329882
SYNPO2
0.925 0.120 4 119028805 intron variant A/C;T snv 2
rs17401966
KIF1B
0.790 0.280 1 10325413 intron variant A/G snv 0.24 7
rs17427875
HOXA11 ; HOXA11-AS
0.925 0.120 7 27185939 non coding transcript exon variant A/T snv 0.15 2
rs17507066
CHEK2
0.925 0.120 22 28696732 intron variant C/T snv 7.0E-02 2
rs17702471
GPC6
0.925 0.120 13 93224864 upstream gene variant A/G snv 0.16 2