Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 13
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03 13
rs9917425
OTOR
20 16755400 intron variant G/T snv 0.16 13
rs7296503
PDZRN4
12 41306962 intron variant C/T snv 0.57 13
rs4837892
TTLL11
9 121826025 intron variant G/T snv 0.36 13
rs174549
FADS2 ; FADS1
0.851 0.240 11 61803910 5 prime UTR variant G/A snv 0.26 12
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 12
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs2179593
TOX2
0.790 0.080 20 44031646 intron variant C/A snv 0.71 11
rs218265 4 54542832 intergenic variant T/C snv 0.21 10
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 10
rs17758695
BCL2
18 63253621 intron variant C/T snv 2.1E-02 10
rs76428106
FLT3
0.851 0.040 13 28029870 intron variant T/C;G snv 10
rs4895441
LOC105378010
0.925 0.080 6 135105435 upstream gene variant A/G snv 0.21 10
rs389884
STK19 ; CYP21A2 ; DXO
0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 10
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
rs150813342
GFI1B
9 132989126 synonymous variant C/T snv 4.1E-03 4.1E-03 9
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 9
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 9
rs1800973
LYZ
0.827 0.320 12 69350234 missense variant C/A snv 4.2E-02 4.3E-02 9
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 9