Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3024912
LOC105373805
0.925 0.120 2 191028361 intron variant A/C snv 0.29 2
rs35771982
PLA2R1
0.925 0.120 2 160028907 missense variant G/C snv 0.39 0.35 2
rs9272729
HLA-DQA2 ; LOC107986589 ; HLA-DQA1
1.000 0.120 6 32641817 intron variant G/A;C snv 1
rs17830558
PLA2R1
1.000 0.120 2 160021853 intron variant T/G snv 0.39 1
rs9267522
PRRC2A
1.000 0.120 6 31635993 synonymous variant A/G snv 1
rs3024877
STAT4
1.000 0.120 2 191040163 intron variant C/T snv 0.35 1
rs3024908
STAT4 ; LOC105373805
1.000 0.120 2 191029415 intron variant T/C snv 9.7E-02 1
rs4326755
TRPC6
1.000 0.120 11 101578627 intron variant G/A snv 0.48 1