Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs750805885
MCL1 ; LOC107985203
0.882 0.080 1 150579475 frameshift variant -/C delins 4.7E-06 3
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
rs848
IL13 ; TH2LCRR
0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67 8
rs281875214
CARD14
0.790 0.160 17 80183976 missense variant A/C snv 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
rs1551399
LOC105375746
0.827 0.120 8 125527723 intron variant A/C snv 0.46 5
rs61802846
FCGR2A
0.827 0.120 1 161504083 upstream gene variant A/C snv 8.8E-02 5
rs371045754
F9
0.882 0.200 X 139530726 upstream gene variant A/C snv 5.5E-06 1.9E-05 4
rs12119179 0.925 0.200 1 67281732 downstream gene variant A/C snv 0.30 2
rs4908742 0.925 0.080 1 8184970 upstream gene variant A/C snv 0.63 2
rs10960680 1.000 0.040 9 12483941 intergenic variant A/C snv 9.4E-02 1
rs1343152
IL23R
1.000 0.040 1 67238649 intron variant A/C snv 0.33 1
rs151823
ERAP1
1.000 0.040 5 96824289 intron variant A/C snv 0.90 1
rs4319543 1.000 0.040 12 122160501 intergenic variant A/C snv 0.35 1
rs514475 1.000 0.040 6 137717768 intron variant A/C snv 0.90 1
rs610037
AP5B1
1.000 0.040 11 65779386 synonymous variant A/C snv 0.45 0.52 1
rs73129298
RNF114
1.000 0.040 20 49949528 intron variant A/C snv 9.2E-02 1
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 12
rs280519
TYK2
0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 10
rs714830
CDKAL1
0.827 0.120 6 20624151 intron variant A/C;G snv 0.13 5
rs7195296 0.827 0.120 16 11655918 intergenic variant A/C;G snv 5
rs27432
ERAP1 ; LOC102724748
0.925 0.040 5 96783569 intron variant A/C;G snv 2