Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs865488
TG
0.882 8 132926377 intron variant C/T snv 0.67 4
rs10425559 0.807 0.040 19 4837475 upstream gene variant A/G snv 0.66 7
rs636393 6 137686393 intron variant G/T snv 0.66 2
rs212402
LOC105378083
1.000 0.080 6 159051263 intron variant G/A snv 0.66 3
rs4675374
ICOS ; LOC101927840
0.882 0.200 2 203937855 intron variant T/C snv 0.65 5
rs1355208 2 30222456 intergenic variant A/G snv 0.65 2
rs1320344
C12orf42
0.882 12 103493699 intron variant A/G snv 0.64 4
rs11086102 0.882 19 18287818 upstream gene variant G/C snv 0.64 6
rs34884278 0.724 0.240 1 172869708 intron variant C/T snv 0.63 14
rs1333739
RAVER2
1 64827766 intron variant A/G;T snv 0.62 1
rs5865
TMEM131
0.851 0.040 2 97756543 3 prime UTR variant C/T snv 0.62 5
rs1126407
LOC107985367 ; LGALS8
0.925 0.200 1 236537507 missense variant T/A snv 0.61 0.61 3
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61 7
rs231804 0.925 0.200 2 203843923 intergenic variant C/T snv 0.60 4
rs3811047
IL37
0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60 10
rs212389
LOC105378083 ; LOC112267968
0.925 0.160 6 159068759 non coding transcript exon variant G/A snv 0.60 4
rs2181622
LINC02656 ; LINC02649
0.882 10 6349099 intron variant G/A snv 0.59 4
rs7042370
LURAP1L-AS1 ; LURAP1L
0.724 0.240 9 12785074 intron variant T/C snv 0.58 14
rs10954213
IRF5
0.752 0.200 7 128949373 3 prime UTR variant G/A snv 0.58 11
rs237025
SUMO4 ; TAB2
0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs12482947
UBASH3A
0.851 0.040 21 42431928 intron variant T/C snv 0.57 5
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13
rs1310182
AP4B1-AS1 ; PTPN22
0.882 0.360 1 113830881 intron variant A/C;G snv 0.56 4
rs2280141
PLEKHA1
1.000 0.040 10 122433665 3 prime UTR variant T/G snv 0.56 4
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5