Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1555876140
SMARCB1
22 23793671 frameshift variant -/C delins 1
rs1673041
POLD1
19 50406132 intron variant T/A;G snv 0.73 0.79 1
rs11979158
EGFR
0.882 0.040 7 55091656 intron variant A/G;T snv 0.20 5
rs1920116
LRRC31
0.882 0.040 3 169862183 intron variant G/A snv 0.25 5
rs2252586 0.882 0.040 7 54911231 intergenic variant C/T snv 0.27 5
rs10852606
HEATR3
0.882 0.040 16 50094961 intron variant T/A;C snv 4
rs11233250
MIR4300HG
0.882 0.040 11 82685972 intron variant C/T snv 0.11 4
rs12230172
LOC105369844
0.882 0.040 12 75848895 intron variant A/G snv 0.48 4
rs12752552
RAVER2
0.882 0.040 1 64763616 intron variant T/C snv 0.13 4
rs1801591
ETFA
0.882 0.040 15 76286421 missense variant G/A snv 7.4E-02 6.4E-02 4
rs2235573
SLC16A8
0.882 0.040 22 38081923 synonymous variant G/A snv 0.47 0.46 4
rs2562152
RHBDF1
0.882 0.040 16 73898 intron variant A/T snv 0.67 4
rs3751667
LMF1
1.000 0.040 16 954554 synonymous variant C/T snv 0.28 0.29 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
rs648044
ZBTB16 ; LOC101928875
0.882 0.040 11 114160077 non coding transcript exon variant A/G;T snv 4
rs723527
EGFR
0.882 0.040 7 55067179 intron variant A/G snv 0.53 4
rs75061358 0.882 0.040 7 54848587 intergenic variant T/C;G snv 4
rs10131032
AKAP6
1.000 0.040 14 32780875 intron variant G/A snv 9.3E-02 2
rs10494090
SLC25A24
1.000 0.040 1 108150714 intron variant A/C;G;T snv 2
rs10924303
LOC105373265 ; KIF26B
1.000 0.040 1 245683732 intron variant C/T snv 0.15 2
rs10924690
SMYD3
1.000 0.040 1 246320481 intron variant G/A snv 0.20 2
rs11163687
LOC107985037
1.000 0.040 1 83199436 intergenic variant A/G snv 9.6E-02 2
rs11166389
SLC35A3 ; RNU6-1318P
1.000 0.040 1 100000723 non coding transcript exon variant G/A snv 0.15 2
rs111696067
GOLGA3
1.000 0.040 12 132799954 intron variant T/C snv 5.3E-04 2