Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 32
rs568408
IL12A ; IL12A-AS1
0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16 29
rs9808753
IFNGR2
0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs872071
IRF4
0.742 0.360 6 411064 3 prime UTR variant A/G;T snv 13
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 11
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 10
rs31490
CLPTM1L
0.776 0.280 5 1344343 splice region variant G/A;T snv 0.37; 8.0E-06 8
rs735665
GRAMD1B
0.776 0.280 11 123490689 intron variant G/A snv 0.15 8
rs1494555
IL7R
0.790 0.120 5 35871088 missense variant G/A snv 0.64 0.72 8
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 7
rs9392504 0.827 0.120 6 412802 downstream gene variant G/A snv 0.44 7
rs9272535
HLA-DQA2 ; LOC107986589 ; HLA-DQA1
0.827 0.280 6 32638979 synonymous variant G/A snv 3.0E-05 1.8E-03 7
rs11755724
RREB1
0.807 0.320 6 7118757 intron variant A/G;T snv 7
rs210143
GGNBP1 ; BAK1
0.827 0.160 6 33579153 intron variant T/C snv 0.74 6
rs6793295
LRRC34
0.827 0.240 3 169800667 missense variant T/C;G snv 0.37; 1.8E-04 6
rs9880772 0.827 0.240 3 27736288 intergenic variant G/A snv 0.59 5
rs4459895
LPP
0.827 0.160 3 188236626 intron variant A/C snv 0.88 5
rs17483466
MIR4435-2HG ; ACOXL
0.827 0.280 2 111039881 intron variant A/G snv 0.15 5
rs13397985
SP110 ; SP140
0.827 0.280 2 230226508 intron variant T/C;G snv 5
rs926070
TSBP1-AS1 ; TSBP1
0.827 0.320 6 32289789 intron variant G/A snv 0.68 5
rs13069553 0.851 0.200 3 169790484 upstream gene variant A/G snv 0.21 4