Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 14
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 9
rs1265115
CCHCR1
0.925 0.080 6 31149298 non coding transcript exon variant C/A;T snv 5
rs3130779 0.925 0.080 6 30904426 upstream gene variant A/C;G;T snv 5
rs3131034
DDR1
0.925 0.080 6 30886019 intron variant G/A snv 0.75 5
rs4148876
TAP2
0.925 0.080 6 32829016 missense variant G/A snv 7.6E-02 5.7E-02 4
rs5745568
GGNBP1 ; BAK1
0.882 0.080 6 33580617 intron variant G/T snv 0.19 4
rs6141
THPO
0.925 0.080 3 184372478 3 prime UTR variant C/G;T snv 4.0E-06; 0.56 4
rs2243873
CYP21A2 ; EHMT2
1.000 0.080 6 31895656 non coding transcript exon variant C/A snv 0.61 3
rs3917267
IL1R1
0.882 0.080 2 102162359 intron variant G/A snv 0.32 3
rs7549785
FCER1A
0.925 0.080 1 159308078 3 prime UTR variant G/A snv 0.13 3
rs12354
LTBR
0.925 0.080 12 6390939 3 prime UTR variant T/A;G snv 1.6E-04; 0.76 2
rs1866139
GNLY
1.000 0.080 2 85694266 intron variant G/C snv 0.51 2
rs201339654
SLC10A1
0.925 0.080 14 69786192 missense variant C/G;T snv 8.0E-06; 2.0E-05 2
rs2256609
UBE2L3
0.925 0.080 22 21570728 intron variant A/G snv 0.18 2
rs2723175
IL37
1.000 0.080 2 112910176 upstream gene variant G/A snv 0.11 2
rs2856726 1.000 0.080 6 32698944 intergenic variant A/T snv 0.34 2
rs2858312 1.000 0.080 6 32699453 intergenic variant G/C snv 0.32 2
rs3135021
HLA-DPB1 ; HLA-DPA1
0.925 0.080 6 33077781 intron variant G/A snv 0.32 2
rs370229832
F2
0.925 0.080 11 46739293 missense variant T/C snv 3.2E-05 6.3E-05 2
rs3806798
IL15
0.925 0.080 4 141636126 upstream gene variant T/A snv 8.7E-02 2
rs4148871
TAP2
0.925 0.080 6 32835539 intron variant A/G snv 0.82 2
rs5751902
GGT1
1.000 0.080 22 24600663 intron variant C/T snv 0.29 2
rs5754344
UBE2L3
1.000 0.080 22 21609497 intron variant A/G snv 0.18 2
rs6472812
LY96
1.000 0.080 8 74004849 missense variant A/G snv 0.97 0.97 2