Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs147856773
FOXO3
1.000 0.040 6 108666024 intron variant -/GGT delins 0.14 1
rs3763313
BTNL2
0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 7
rs17780256
LOC105371887 ; SLC39A11
0.827 0.120 17 72646784 3 prime UTR variant A/C snv 0.18 6
rs10775412
KSR1
0.827 0.120 17 27542007 intron variant A/C snv 0.30 5
rs1517352
STAT4
0.851 0.160 2 191066738 intron variant A/C snv 0.45 5
rs1551399
LOC105375746
0.827 0.120 8 125527723 intron variant A/C snv 0.46 5
rs360718
IL18
0.827 0.120 11 112164016 5 prime UTR variant A/C snv 0.26 5
rs61802846
FCGR2A
0.827 0.120 1 161504083 upstream gene variant A/C snv 8.8E-02 5
rs72796353
NOD2
0.882 0.080 16 50712383 3 prime UTR variant A/C snv 1.3E-02 1.4E-02 5
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 4
rs3814057
NR1I2
0.925 0.040 3 119818407 3 prime UTR variant A/C snv 0.28 4
rs12948909
CAVIN1
0.925 0.120 17 42418584 intron variant A/C snv 0.24 3
rs2382817
PNKD ; TMBIM1
0.925 0.040 2 218286495 5 prime UTR variant A/C snv 0.61 3
rs3135499
NOD2
0.882 0.160 16 50732216 splice donor variant A/C snv 0.45 3
rs9891119
STAT3
0.882 0.120 17 42355962 intron variant A/C snv 0.36 3
rs11167764
LOC105378204
0.925 0.120 5 142099500 regulatory region variant A/C snv 0.80 2
rs4807569
SBNO2
0.925 0.120 19 1123379 intron variant A/C snv 0.25 2
rs7165170
CRTC3-AS1 ; CRTC3
1.000 0.040 15 90638257 non coding transcript exon variant A/C snv 0.26 2
rs104895469
NOD2
1.000 0.040 16 50710981 missense variant A/C snv 2.4E-04 1.5E-04 1
rs13371189 1.000 0.040 18 11304692 intergenic variant A/C snv 1
rs140068907 1.000 0.040 6 32691666 regulatory region variant A/C snv 3.4E-03 1
rs16853571
PHOX2B-AS1
1.000 0.040 4 41751113 intron variant A/C snv 9.9E-02 1
rs16931910
DELEC1
1.000 0.040 9 114856029 intron variant A/C snv 7.2E-02 1
rs17312836
NOD2
1.000 0.040 16 50707551 intron variant A/C snv 0.33 1
rs247660 1.000 0.040 5 85462322 upstream gene variant A/C snv 0.21 1