Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs56302315
KDR
0.827 0.160 4 55089802 missense variant C/T snv 5.3E-04 4.1E-04 5
rs3212227
IL12B
0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs10719
DROSHA
0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
rs644236
DROSHA
0.882 0.320 5 31409008 non coding transcript exon variant T/C snv 0.31 0.35 5
rs2546191
ELL2
0.851 0.160 5 95896837 intron variant G/A snv 0.38 4
rs2069757
TH2LCRR
1.000 0.120 5 132662721 intron variant G/A snv 7.5E-02 1
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs4746
GLO1
0.708 0.400 6 38682852 missense variant T/A;G snv 0.36 21
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs872071
IRF4
0.742 0.360 6 411064 3 prime UTR variant A/G;T snv 13
rs2516049
HLA-DRB1
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 12
rs6903608
HLA-DRB9
0.742 0.400 6 32460508 intron variant C/G;T snv 11
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 10
rs477515
HLA-DRB1
0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 10
rs3763313
BTNL2
0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 7
rs805303
BAG6
0.925 0.160 6 31648589 intron variant G/A snv 0.45 7
rs210143
GGNBP1 ; BAK1
0.827 0.160 6 33579153 intron variant T/C snv 0.74 6
rs2534657
MICB
0.882 0.200 6 31504682 intron variant C/T snv 0.15 6
rs3129882
HLA-DRA
0.807 0.240 6 32441753 intron variant G/A snv 0.56 6
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 6
rs9268403
TSBP1 ; TSBP1-AS1
0.807 0.240 6 32373696 intron variant T/C snv 0.24 6
rs204993
PBX2
0.851 0.240 6 32187804 intron variant A/G snv 0.24 0.26 5