Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10885
PRRC2A
6 31636814 missense variant C/T snv 0.14 0.17 1
rs2153486 14 87737048 intron variant C/T snv 0.68 1
rs3130623
PRRC2A
6 31629923 intron variant C/T snv 0.18 1
rs314879 13 22735243 intergenic variant C/T snv 0.78 1
rs6105452
MACROD2
20 15683126 intron variant C/T snv 0.10 1
rs6797827 3 109735523 intron variant C/T snv 0.18 1
rs9405108
HLA-DRB9
6 32470871 intron variant C/T snv 0.29 1
rs477515
HLA-DRB1
0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 10
rs7194
HLA-DRA
0.827 0.280 6 32444703 3 prime UTR variant G/A snv 0.61 7
rs1048369
GPC4
0.882 0.160 X 133303309 missense variant G/A snv 0.33 0.38 4
rs2227139 0.925 0.160 6 32445682 downstream gene variant G/A snv 0.61 4
rs3129888
HLA-DRA
0.882 0.240 6 32443949 intron variant G/A snv 0.82 0.80 4
rs2213585
HLA-DRA
1.000 0.040 6 32445373 downstream gene variant G/A snv 0.61 2
rs28362683
BTNL2 ; TSBP1-AS1
1.000 0.040 6 32405186 synonymous variant G/A snv 0.12 0.10 2
rs1062630
POU5F1
6 31170330 synonymous variant G/A snv 0.18 0.22 1
rs1161098
LOC105369812 ; LINC02408
12 67453680 intron variant G/A snv 0.84 1
rs204992
PBX2
6 32189131 intron variant G/A snv 0.22 1
rs28362680
BTNL2 ; TSBP1-AS1
6 32403039 missense variant G/A snv 0.14 0.12 1
rs594418
NRG3
10 82625296 intron variant G/A snv 0.83 1
rs9268658
HLA-DRA
1.000 0.040 6 32442939 intron variant G/A;C snv 2
rs200655768
TTN-AS1 ; TTN
2 178711222 synonymous variant G/A;T snv 1
rs62309385 4 136134743 intron variant G/C snv 9.8E-02 1
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs2395182
HLA-DRA
0.851 0.280 6 32445540 downstream gene variant G/T snv 0.76 5
rs10947261
BTNL2 ; TSBP1-AS1
0.882 0.240 6 32405455 splice region variant G/T snv 0.11 4