Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs660895
HLA-DRB1
0.752 0.360 6 32609603 intergenic variant A/G snv 0.19 10
rs9275596 0.827 0.280 6 32713854 upstream gene variant C/T snv 0.66 7
rs9275224 0.851 0.200 6 32692101 TF binding site variant A/G snv 0.53 5
rs4664308
LOC105373717 ; PLA2R1
0.851 0.160 2 160060986 intron variant A/G snv 0.30 4
rs35771982
PLA2R1
0.925 0.120 2 160028907 missense variant G/C snv 0.39 0.35 2
rs28383345
HLA-DQA2 ; LOC107986589 ; HLA-DQA1
1.000 0.120 6 32637457 5 prime UTR variant G/A snv 9.4E-02 0.12 1
rs2715928
LOC105373717 ; PLA2R1
1.000 0.120 2 160057088 intron variant A/G snv 0.64 1
rs2715918
PLA2R1
1.000 0.120 2 159976677 splice region variant A/G;T snv 0.82 1
rs3749119
PLA2R1
1.000 0.120 2 160062509 5 prime UTR variant C/T snv 0.26 1
rs16844715
PLA2R1 ; LOC105373717
1.000 0.120 2 160058595 intron variant C/T snv 0.31 1
rs875
PPP3R1
1.000 0.120 2 68180794 3 prime UTR variant A/G;T snv 0.29 1