Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs112209031
HLA-DRB5 ; HLA-DRB3
1.000 0.040 6 32524630 intron variant T/C;G snv 2
rs11223651 1.000 0.040 11 133971139 intergenic variant C/T snv 0.16 2
rs112635299
SERPINA2
1.000 0.040 14 94371805 downstream gene variant G/T snv 1.3E-02 7
rs1131275
MIR6891 ; HLA-B
1.000 0.040 6 31356183 missense variant G/A;C snv 0.68 2
rs113205291
HLA-A
1.000 0.040 6 29894844 upstream gene variant A/G;T snv 2
rs113397282
HLA-DRB3 ; HLA-DRB5
1.000 0.040 6 32520273 intron variant T/C;G snv 2
rs113764414
EGR2
10 62889636 intron variant A/G snv 3.6E-04 1
rs114041423 1.000 0.040 6 29639270 upstream gene variant G/A snv 2
rs114086406
TSBP1-AS1
1.000 0.040 6 32374760 intron variant G/A snv 2
rs114115252
SFTA2
1.000 0.040 6 30931418 3 prime UTR variant G/A;C;T snv 2
rs114142645 1.000 0.040 6 31245806 regulatory region variant T/C snv 2
rs114204022
HLA-A
1.000 0.040 6 29972902 upstream gene variant G/A snv 2
rs114274203
LINC02571 ; HLA-B ; LOC112267902
1.000 0.040 6 31300843 intron variant C/T snv 2
rs114276265 1.000 0.040 6 31219298 upstream gene variant C/T snv 2
rs114277634
HCP5
1.000 0.040 6 31474954 intron variant T/A;C snv 2
rs114291394 1.000 0.040 6 31383745 upstream gene variant A/C snv 2
rs114441450
TUBB ; MDC1
1.000 0.040 6 30719037 upstream gene variant G/A;T snv 2
rs114455101
HLA-DRB9
1.000 0.040 6 32465853 intron variant T/G snv 2
rs114508985 1.000 0.040 6 32932241 downstream gene variant C/G;T snv 2
rs114771361
MTCO3P1
1.000 0.040 6 32706552 non coding transcript exon variant G/A snv 2
rs114810457
PBX2
1.000 0.040 6 32186508 non coding transcript exon variant A/G snv 2
rs114812317
HLA-DRB5
1.000 0.040 6 32531497 upstream gene variant G/A snv 2
rs114830752 1.000 0.040 6 32715035 upstream gene variant C/A snv 2
rs114838832
MUCL3 ; SFTA2
1.000 0.040 6 30937536 intron variant A/G snv 2
rs114867672 1.000 0.040 6 30964067 upstream gene variant T/C snv 2