Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11465797
IL23R ; C1orf141
1.000 0.040 1 67200769 missense variant C/A snv 2
rs2488397
DENND1B
1.000 0.040 1 197732149 intron variant G/C snv 0.23 2
rs2501846 1.000 0.040 1 212668592 upstream gene variant T/C snv 0.24 2
rs2651244 1.000 0.040 1 70529879 upstream gene variant G/A snv 0.30 2
rs3180018
SCAMP3
1.000 0.040 1 155260340 synonymous variant C/T snv 2
rs35675666
PARK7
1.000 0.040 1 7961913 5 prime UTR variant G/C;T snv 2
rs59043219
IRF6
1.000 0.040 1 209797265 intron variant G/A snv 0.36 2
rs7517810 1.000 0.040 1 172884320 intron variant C/T snv 0.29 2
rs7555082 1.000 0.040 1 198629533 intergenic variant G/A snv 8.4E-02 2
rs1343126
MAGI3
1 113586470 intron variant A/T snv 0.25 1
rs2297559
ITLN1
1 160884736 intron variant G/A snv 0.66 1
rs34856868
BTBD8
1 92088726 missense variant G/A snv 2.0E-02 2.0E-02 1
rs35730213
INAVA
1 200905101 intron variant G/C snv 0.22 1
rs3766920
LOC101928120 ; SHC1 ; PYGO2
1 154962487 3 prime UTR variant G/A snv 1.2E-03 1
rs490608
DAP3
1 155713079 intron variant C/T snv 0.48 1
rs6689879
MAGI3
1 113559097 intron variant T/C snv 0.29 1
rs72634258 1 8090578 intron variant T/C snv 0.13 1
rs7547569 1 67265685 downstream gene variant T/C snv 4.7E-02 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs2292832
MIR149 ; GPC1 ; LOC100130449
0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs2241880
SCARNA5 ; ATG16L1
0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37