Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs71305152
ZFPM2
0.882 0.040 8 105437494 intron variant -/TTTTCT delins 0.43 5
rs2239647
AKAP6
0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65 7
rs374524467
PITX2
0.827 0.040 4 110632961 missense variant A/C snv 8.0E-06 7.0E-06 5
rs865880036
MEIS2
0.827 0.040 15 37098156 missense variant A/C snv 1.3E-04 5
rs9933544 0.882 0.040 16 24576962 downstream gene variant A/C snv 0.29 3
rs11216930
PHLDB1
1.000 0.040 11 118618067 intron variant A/C snv 0.22 2
rs730437
EGFR
0.925 0.120 7 55147325 intron variant A/C snv 0.51 2
rs201963
ADAM18
1.000 0.040 8 39721376 intron variant A/C snv 1
rs3212112
XRCC3 ; KLC1
1.000 0.040 14 103699345 intron variant A/C snv 7.1E-03 2.2E-02 1
rs4774756
RAB27A
1.000 0.040 15 55254859 intron variant A/C snv 0.66 1
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs17006625
KAT2B
0.925 0.080 3 20119604 missense variant A/C;G snv 4.0E-06; 3.3E-02 3
rs11706832
LRIG1
1.000 0.040 3 66452557 intron variant A/C;G snv 2
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
rs10494090
SLC25A24
1.000 0.040 1 108150714 intron variant A/C;G;T snv 2
rs1064794096
KLLN ; PTEN
1.000 0.040 10 87864514 missense variant A/C;T snv 2
rs11571378
RAD52
0.925 0.080 12 950115 intron variant A/C;T snv 2
rs1345354331
GPX1
1.000 0.040 3 49358221 missense variant A/C;T snv 6.8E-06; 6.8E-06 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70