Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2778031 1.000 0.040 9 88220811 intergenic variant T/A;C snv 3
rs9504361
EXOC2
1.000 0.040 6 577820 intron variant A/G snv 0.40 3
rs10782001
FBXL19
1.000 0.040 16 30931304 intron variant G/A snv 0.53 2
rs10789285 1.000 0.040 1 69322799 intergenic variant T/G snv 0.33 2
rs12602912
BPTF
1.000 0.040 17 67873957 intron variant C/G;T snv 2
rs13708
STX1B ; HSD3B7
1.000 0.040 16 30989488 3 prime UTR variant G/A;C snv 0.52 2
rs1473247
RNF145
1.000 0.040 5 159176563 intron variant T/C snv 0.41 2
rs1713239
IL20
1.000 0.040 1 206864130 upstream gene variant G/C snv 0.88 2
rs201909740
CD28
1.000 0.040 2 203734889 missense variant G/A snv 4.0E-06 1.4E-05 2
rs61871342
BLOC1S2
1.000 0.040 10 100278884 intron variant G/A snv 0.36 2
rs67384697
HLA-C
1.000 0.040 6 31268906 3 prime UTR variant C/- delins 6.2E-04 2
rs887466
POU5F1 ; PSORS1C3
1.000 0.040 6 31175734 intron variant G/A snv 0.40 2
rs1002212321
RIMS2
1.000 0.040 8 103931366 missense variant T/C snv 1
rs10088247
CSMD1
1.000 0.040 8 3826677 intron variant C/T snv 0.76 1
rs1008953 1.000 0.040 20 45352086 upstream gene variant T/C snv 0.79 1
rs10180391
GNLY
1.000 0.040 2 85699222 downstream gene variant C/T snv 0.31 1
rs10405308 1.000 0.040 19 1312729 intergenic variant G/A snv 7.9E-02 1
rs10489628
IL23R
1.000 0.040 1 67238424 intron variant G/A snv 0.43 1
rs10515778
LINC01932
1.000 0.040 5 159231004 intron variant A/G snv 0.13 1
rs1051738
PDE4A
1.000 0.040 19 10467167 missense variant C/A;T snv 0.17; 4.8E-05 1
rs10789229
IL23R
1.000 0.040 1 67239891 intron variant C/T snv 0.62 1
rs10794648 1.000 0.040 1 24191716 upstream gene variant T/C snv 0.68 1
rs10888501
LCE3E
1.000 0.040 1 152565478 downstream gene variant G/A snv 0.48 1
rs10960680 1.000 0.040 9 12483941 intergenic variant A/C snv 9.4E-02 1
rs10979182
LOC105376214
1.000 0.040 9 108054739 regulatory region variant A/G snv 0.44 1