Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 11
rs17758695
BCL2
18 63253621 intron variant C/T snv 2.1E-02 10
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs218265 4 54542832 intergenic variant T/C snv 0.21 10
rs9977672 0.827 0.120 21 39091357 intergenic variant G/A snv 0.22 10
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 9
rs2954031 8 125479491 intron variant G/T snv 0.42 9
rs35979828
NFE2
12 54292096 intron variant C/T snv 5.0E-02 9
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 9
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 9
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs35850753
TP53
0.807 0.080 17 7675353 5 prime UTR variant C/T snv 1.3E-02 8
rs3865444
CD33
0.851 0.160 19 51224706 upstream gene variant C/A snv 0.25 8
rs6740847 0.925 0.040 2 181443625 intergenic variant A/G snv 0.57 8
rs8179
CDK6
0.882 0.080 7 92606850 3 prime UTR variant T/A;C;G snv 8
rs9532434
COG6
0.807 0.120 13 39781776 intron variant T/A;C snv 8
rs10810657 0.827 0.080 9 16884588 regulatory region variant T/A;G snv 7
rs12266014
PRTFDC1
10 24922362 intron variant C/T snv 0.26 7
rs2038700
STXBP6
14 24992783 intron variant T/C snv 0.53 7
rs36115365 0.807 0.160 5 1313127 upstream gene variant G/A;C;T snv 7
rs3731211
CDKN2A
9 21986848 intron variant T/A snv 0.74 7
rs60600003
ELMO1
0.827 0.120 7 37342861 intron variant T/C;G snv 7