Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 10
rs1881457
IL13 ; TH2LCRR
0.790 0.280 5 132656717 intron variant A/C snv 0.21 9
rs1057519729
MAP2K1
0.827 0.080 15 66435113 missense variant A/C snv 6
rs1470579
IGF2BP2
0.925 0.160 3 185811292 intron variant A/C snv 0.46 5
rs863225283
ALK
0.925 0.080 2 29213993 missense variant A/C snv 4
rs1711972
FOXF2 ; LOC105374880
0.925 0.160 6 1388953 upstream gene variant A/C snv 4.7E-02 3
rs11622887
SYNE3
1.000 0.080 14 95476110 upstream gene variant A/C snv 0.52 2
rs707467
PER3
0.925 0.120 1 7801624 intron variant A/C snv 0.22 2
rs11574852
NFKB2
1.000 0.080 10 102401718 intron variant A/C snv 2.3E-02 2.3E-02 1
rs61761074
KRAS
1.000 0.080 12 25244659 intron variant A/C snv 2.7E-02 1
rs751648572
SOD2
1.000 0.080 6 159682631 missense variant A/C snv 4.1E-06 1
rs984755949
COL11A2
1.000 0.080 6 33172302 missense variant A/C snv 1
rs213210
MIR219A1 ; RING1
0.742 0.240 6 33208047 upstream gene variant A/C;G snv 11
rs11788747
RECK
0.851 0.240 9 36105267 synonymous variant A/C;G snv 4.0E-06; 0.34 6
rs3756585
SNORD95 ; RACK1
1.000 0.080 5 181244029 intron variant A/C;G snv 0.13 1
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs587782289
TP53
0.752 0.240 17 7674257 missense variant A/C;G;T snv 15
rs281864719
ALK
0.763 0.240 2 29220831 missense variant A/C;G;T snv 14
rs1804429
CXCL12
1.000 0.080 10 44370393 3 prime UTR variant A/C;G;T snv 1
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs3756712
PDCD6 ; AHRR
0.790 0.160 5 308981 non coding transcript exon variant A/C;T snv 10