Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs699473
SOD3
0.827 0.160 4 24795181 intron variant C/T snv 0.54 5
rs71305152
ZFPM2
0.882 0.040 8 105437494 intron variant -/TTTTCT delins 0.43 5
rs891835
CCDC26
0.851 0.120 8 129479506 intron variant T/G snv 0.17 5
rs944797
CDKN2B-AS1
0.882 0.120 9 22115287 intron variant T/C;G snv 0.49 5
rs10852606
HEATR3
0.882 0.040 16 50094961 intron variant T/A;C snv 4
rs10892258
LOC105369519
0.925 0.120 11 118709156 intron variant G/A snv 0.19 4
rs11079041
STAT5B
0.882 0.040 17 42262061 intron variant T/A;C snv 0.36 4
rs11233250
MIR4300HG
0.882 0.040 11 82685972 intron variant C/T snv 0.11 4
rs11506105
EGFR
0.851 0.160 7 55152484 intron variant A/G snv 0.59 4
rs12230172
LOC105369844
0.882 0.040 12 75848895 intron variant A/G snv 0.48 4
rs12615793
ACYP2
0.851 0.280 2 54248777 intron variant G/A;T snv 4
rs12752552
RAVER2
0.882 0.040 1 64763616 intron variant T/C snv 0.13 4
rs2562152
RHBDF1
0.882 0.040 16 73898 intron variant A/T snv 0.67 4
rs3791675
EFEMP1
1.000 0.040 2 55884174 intron variant C/T snv 0.20 4
rs3851634
POLR3B
0.882 0.040 12 106419124 intron variant T/C snv 0.22 4
rs59060240
EGFR
0.882 0.040 7 55080369 intron variant AA/-;A;AAA;AAAA;AAAAAAAAAAA delins 4
rs6489769
RAD52
0.851 0.120 12 963799 intron variant C/A;T snv 4
rs723527
EGFR
0.882 0.040 7 55067179 intron variant A/G snv 0.53 4
rs10464870
CCDC26
0.882 0.040 8 129465577 intron variant C/T snv 0.80 3
rs11603023
PHLDB1
0.925 0.120 11 118615352 intron variant T/C snv 0.57 3
rs117677079
ANXA5
0.882 0.040 4 121673909 intron variant T/C snv 8.3E-03 3
rs145929329
CDKN2B-AS1
0.882 0.040 9 22066213 intron variant TTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTTTTT delins 0.58 3
rs17172432
EGFR
0.882 0.080 7 55073624 intron variant T/C snv 0.31 3
rs2033214
RBBP6
0.882 0.040 16 24566199 intron variant T/G snv 0.14 3
rs2847153
TYMS
0.925 0.080 18 661647 intron variant G/A snv 0.22 3