Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6933404 0.925 0.280 6 137638098 intergenic variant T/C snv 0.16 5
rs3135394
HLA-DRA
0.851 0.240 6 32440720 intron variant A/G snv 6.3E-02 4
rs115575857 1.000 0.200 6 32691868 regulatory region variant A/G snv 1
rs1507153 1.000 0.200 6 78774669 intergenic variant C/A snv 0.32 1
rs9271573 1.000 0.200 6 32622724 TF binding site variant A/C snv 0.55 1
rs117026326
LOC101926943 ; GTF2I
0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10
rs3757387
IRF5
0.851 0.280 7 128936032 upstream gene variant T/C snv 0.38 6
rs7341475
RELN
0.851 0.240 7 103764368 intron variant G/A snv 0.17 6
rs3823536
IRF5
0.925 0.280 7 128939612 intron variant G/A snv 0.40 2
rs17339836
TNPO3
1.000 0.200 7 129041008 intron variant C/T snv 9.0E-02 1
rs2736345
BLK
0.882 0.280 8 11494976 intron variant A/G snv 0.35 3
rs1085308048
PTEN
0.851 0.320 10 87933175 stop gained T/G snv 6
rs7119038 1.000 0.200 11 118867572 intergenic variant G/A snv 0.77 1
rs10774671
OAS1
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs11048434
KLRG1
1.000 0.200 12 9001336 intron variant G/A snv 0.28 1
rs116855232
NUDT15
0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 12
rs17074492
LOC105370283
1.000 0.200 13 81587764 intergenic variant C/A;T snv 1
rs7999279 1.000 0.200 13 47376590 intergenic variant A/C snv 0.76 1
rs774359492
WDHD1
0.807 0.200 14 55008684 missense variant C/T snv 4.0E-06 7.0E-06 7
rs1957173 1.000 0.200 14 45937713 intron variant C/T snv 4.6E-02 1
rs9938751
SHISA9
1.000 0.200 16 12908502 missense variant T/A;C snv 0.88 1
rs61756766
TNFRSF13C
0.776 0.320 22 41925447 missense variant G/A snv 5.7E-03 5.7E-03 9