Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs114882497 1.000 0.040 6 32423415 intergenic variant T/C snv 2
rs114904464 1.000 0.040 6 31380300 upstream gene variant G/A snv 2
rs114950038
HLA-A
1.000 0.040 6 29983056 downstream gene variant G/A;C snv 2
rs114963521
HCG20
1.000 0.040 6 30791080 intron variant C/T snv 2
rs114964506
LINC00243
1.000 0.040 6 30814428 non coding transcript exon variant G/C snv 2
rs115035678
TSBP1-AS1
1.000 0.040 6 32381780 intron variant A/T snv 2
rs115052633
SNORA38 ; PRRC2A
1.000 0.040 6 31621487 intron variant C/G;T snv 2