Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3130618
CSNK2B ; GPANK1
0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 7
rs2239804
HLA-DRA
0.851 0.240 6 32443746 intron variant T/A;C snv 0.51 5
rs2239802
HLA-DRA
0.882 0.200 6 32444069 intron variant C/A;G;T snv 4
rs12759054
SLC35F3
1.000 0.040 1 233984064 intron variant T/A;C snv 3
rs28366298
HLA-DRB1
0.925 0.120 6 32593082 upstream gene variant A/C;T snv 3
rs4935356
HLA-DRA
1.000 0.080 6 32444611 intron variant T/A;G snv 2
rs6901541 1.000 0.120 6 32474484 upstream gene variant T/C;G snv 2
rs8084
HLA-DRA
1.000 0.120 6 32443258 splice acceptor variant A/C;T snv 0.61; 8.1E-06 2
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
rs200688486 6 32621223 regulatory region variant -/T delins 1
rs5861895 4 129344228 regulatory region variant TT/-;T;TTT delins 1
rs80274284
SLC22A15
1 116037356 missense variant G/T snv 1
rs116671518
DKK2
4 107189709 intron variant T/C snv 1.9E-02 1
rs138117677 16 3348899 TF binding site variant GGGACT/- delins 2.8E-02 1
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
rs2854275
HLA-DQB1 ; HLA-DQB1-AS1
0.925 0.120 6 32660651 non coding transcript exon variant C/A snv 9.6E-02 4
rs62309385 4 136134743 intron variant G/C snv 9.8E-02 1
rs6105452
MACROD2
20 15683126 intron variant C/T snv 0.10 1
rs28362683
BTNL2 ; TSBP1-AS1
1.000 0.040 6 32405186 synonymous variant G/A snv 0.12 0.10 2
rs10947261
BTNL2 ; TSBP1-AS1
0.882 0.240 6 32405455 splice region variant G/T snv 0.11 4
rs28362680
BTNL2 ; TSBP1-AS1
6 32403039 missense variant G/A snv 0.14 0.12 1
rs10947262
TSBP1-AS1 ; BTNL2
0.925 0.040 6 32405535 non coding transcript exon variant C/T snv 0.12 3
rs10885
PRRC2A
6 31636814 missense variant C/T snv 0.14 0.17 1