Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9577873
GAS6 ; GAS6-AS1
1.000 0.200 13 113825282 intron variant G/A;T snv 1
rs9517723
LOC107984558
0.925 0.200 13 99432425 non coding transcript exon variant T/C snv 0.65 2
rs9517701
UBAC2
1.000 0.200 13 99377286 3 prime UTR variant A/G snv 0.13 1
rs9517668
UBAC2
1.000 0.200 13 99271586 intron variant T/A snv 0.80 1
rs9513584
UBAC2
1.000 0.200 13 99224027 intron variant G/A snv 0.57 1
rs9494885
LOC107986649 ; WAKMAR2
0.882 0.320 6 137851611 intron variant T/C snv 0.20 3
rs947474
LINC02649 ; LINC02656
0.827 0.440 10 6348488 intron variant G/A snv 0.79 5
rs9471535
TREM1
0.851 0.240 6 41287752 upstream gene variant T/C snv 0.12 5
rs943899383
F5
1.000 0.200 1 169586343 frameshift variant C/- delins 1
rs9380217 1.000 0.200 6 31083776 downstream gene variant C/T snv 6.4E-02 1
rs9368678
LOC112267902 ; HLA-B
1.000 0.200 6 31304686 intron variant T/C snv 9.2E-02 1
rs936551
CPLX1
1.000 0.200 4 827702 upstream gene variant A/G snv 0.52 1
rs9316059
NRAD1 ; LOC107984576
1.000 0.200 13 43912653 intron variant A/C;T snv 1
rs9268861
HLA-DRB9
0.925 0.280 6 32462117 intron variant C/A snv 0.22 2
rs9266490 1.000 0.200 6 31372381 intron variant A/G snv 0.22 1
rs9266409 0.925 0.200 6 31368791 intron variant T/C snv 0.22 5
rs9266406 1.000 0.200 6 31368641 intron variant G/A snv 0.22 1
rs9260997
HLA-A
1.000 0.200 6 29995539 upstream gene variant T/C snv 0.90 1
rs924080 0.882 0.240 1 67294457 intergenic variant T/C snv 0.45 3
rs913678 0.882 0.240 20 50338887 regulatory region variant T/C snv 0.51 6
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs897200
STAT4
0.851 0.280 2 191153045 upstream gene variant T/C snv 0.54 4
rs886040969
NOD2
1.000 0.200 16 50712357 missense variant G/A snv 1
rs886039866
TNFRSF1A
1.000 0.200 12 6333376 missense variant G/A snv 1
rs855873
AIM2
1.000 0.200 1 159077922 intron variant A/G snv 0.84 1