Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1015166
TAP2
0.925 0.120 6 32830954 intron variant C/G;T snv 0.28 2
rs1133076
TG
0.925 0.080 8 133113438 missense variant G/A snv 0.48 0.56 2
rs2358994
BCL2L15 ; AP4B1-AS1
0.925 0.120 1 113886839 intron variant G/A snv 0.16 2
rs7679475
LOC107986309
0.925 0.120 4 121392885 intergenic variant A/C;G snv 2
rs13093110
LPP
0.882 0.120 3 188407332 intron variant C/T snv 0.42 4
rs11571297 0.882 0.120 2 203880280 regulatory region variant T/C snv 0.44 3
rs57348955 0.882 0.120 16 31174561 upstream gene variant G/A;C snv 3
rs7537605
VAV3
0.882 0.120 1 107800465 intron variant G/A;T snv 3
rs17759659
BCL2
0.851 0.120 18 63291411 intron variant A/G snv 0.31 4
rs2857595 0.827 0.320 6 31600692 intergenic variant G/A snv 0.27 9
rs121434257
AIRE
0.827 0.080 21 44289686 missense variant G/A;T snv 4.0E-05 6
rs1534422
MIR3681HG
0.827 0.160 2 12500615 intron variant G/A snv 0.52 6
rs2251396
MICA-AS1
0.827 0.240 6 31396930 upstream gene variant G/A snv 0.24 5
rs2270450
LOC101926934 ; SLC25A27
0.827 0.200 6 46677138 3 prime UTR variant C/T snv 0.29 5
rs2523989
TRIM31 ; TRIM31-AS1
0.827 0.280 6 30110498 missense variant C/T snv 0.12 0.12 5
rs706779
IL2RA
0.827 0.160 10 6056861 intron variant T/C snv 0.48 5
rs2153977
MAGI3
0.807 0.240 1 113537449 intron variant C/T snv 0.28 6
rs1980493
BTNL2 ; TSBP1-AS1
0.776 0.400 6 32395438 intron variant T/C snv 0.13 10
rs886424
LINC00243
0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 10
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs1270942
CFB ; CYP21A2
0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 11
rs1689510
SUOX
0.724 0.240 12 56002984 non coding transcript exon variant G/C snv 0.25 16
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15
rs12928404
ATXN2L
0.724 0.240 16 28835925 splice region variant T/C snv 0.44 0.45 15
rs2836882 0.724 0.240 21 39094644 intergenic variant G/A snv 0.23 15