Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 14
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs4837892
TTLL11
9 121826025 intron variant G/T snv 0.36 13
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs7296503
PDZRN4
12 41306962 intron variant C/T snv 0.57 13
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03 13
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs9917425
OTOR
20 16755400 intron variant G/T snv 0.16 13
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs76428106
FLT3
0.851 0.040 13 28029870 intron variant T/C;G snv 10
rs35979828
NFE2
12 54292096 intron variant C/T snv 5.0E-02 9
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 7
rs12679834
LPL
8 19962922 intron variant T/C snv 9.4E-02 7
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 7
rs3731211
CDKN2A
9 21986848 intron variant T/A snv 0.74 7
rs3747207
PNPLA3
22 43928975 intron variant G/A snv 0.22 7