Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9405108
HLA-DRB9
6 32470871 intron variant C/T snv 0.29 1
rs9368726
HLA-DRB9
6 32470765 intron variant T/C snv 0.29 1
rs9271488 6 32621223 regulatory region variant G/T snv 0.27 1
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 10
rs9268832
HLA-DRB9
0.882 0.160 6 32460012 non coding transcript exon variant T/C snv 0.61 0.59 4
rs9268658
HLA-DRA
1.000 0.040 6 32442939 intron variant G/A;C snv 2
rs9267536
LOC105375019 ; LY6G5C
6 31683417 intron variant A/C snv 5.3E-02 1
rs9267532
LY6G5B ; CSNK2B
1.000 0.120 6 31672202 missense variant C/T snv 7.4E-02 7.9E-02 2
rs8084
HLA-DRA
1.000 0.120 6 32443258 splice acceptor variant A/C;T snv 0.61; 8.1E-06 2
rs80274284
SLC22A15
1 116037356 missense variant G/T snv 1
rs7754768 1.000 0.040 6 32452402 regulatory region variant C/T snv 0.56 2
rs7195
HLA-DRA
1.000 0.040 6 32444762 3 prime UTR variant A/G snv 0.61 2
rs7194
HLA-DRA
0.827 0.280 6 32444703 3 prime UTR variant G/A snv 0.61 7
rs7192
HLA-DRA
0.827 0.200 6 32443869 missense variant T/G snv 0.64 0.61 7
rs6901541 1.000 0.120 6 32474484 upstream gene variant T/C;G snv 2
rs6797827 3 109735523 intron variant C/T snv 0.18 1
rs652888
EHMT2-AS1 ; EHMT2 ; LOC107986588 ; CYP21A2
0.776 0.480 6 31883457 non coding transcript exon variant A/G snv 0.18 0.20 10
rs62309385 4 136134743 intron variant G/C snv 9.8E-02 1
rs6105452
MACROD2
20 15683126 intron variant C/T snv 0.10 1
rs594418
NRG3
10 82625296 intron variant G/A snv 0.83 1
rs5861895 4 129344228 regulatory region variant TT/-;T;TTT delins 1
rs4935356
HLA-DRA
1.000 0.080 6 32444611 intron variant T/A;G snv 2
rs4919510
SEMA4G ; MIR608 ; MRPL43
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs477515
HLA-DRB1
0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 10
rs4248166
TSBP1-AS1 ; BTNL2
1.000 0.040 6 32398644 intron variant T/C snv 0.18 2