Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4948088 0.925 0.160 7 50959497 intron variant A/C snv 0.96 2
rs1050391
HLA-DMB ; HLA-DMA
1.000 0.080 6 32950080 non coding transcript exon variant A/G snv 0.93 1
rs3129305 1.000 0.080 6 32991403 intergenic variant G/C snv 0.93 1
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs3130933
POU5F1 ; TCF19
0.882 0.200 6 31164308 intron variant T/C snv 0.92 2
rs2670117
KCNMA1
1.000 0.080 10 77594713 intron variant A/G snv 0.91 1
rs9267658
CYP21A2 ; SLC44A4 ; EHMT2-AS1
0.882 0.240 6 31878208 intron variant T/C snv 0.91 3
rs3132946
NOTCH4
0.882 0.240 6 32222251 intron variant A/G snv 0.91 3
rs2736177 1.000 0.080 6 31618317 upstream gene variant C/T snv 0.91 1
rs3131294
NOTCH4
1.000 0.080 6 32212369 intron variant A/G snv 0.91 1
rs3134954
TNXB
0.882 0.240 6 32104116 intron variant C/T snv 0.90 3
rs3130287
TNXB
1.000 0.080 6 32082767 intron variant C/T snv 0.90 1
rs3135388
HLA-DRA
0.807 0.240 6 32445274 downstream gene variant A/G snv 0.90 1
rs3130050
APOM ; BAG6
0.882 0.240 6 31650984 intron variant G/A snv 0.89 3
rs9267992 0.882 0.240 6 32252620 upstream gene variant G/A snv 0.89 3
rs3094609
HCG27
0.925 0.080 6 31197789 non coding transcript exon variant T/C snv 0.86 0.89 5
rs3130532 1.000 0.080 6 31240676 intergenic variant A/G snv 0.88 1
rs3130952 1.000 0.080 6 31210138 intergenic variant G/A snv 0.88 1
rs9267649 0.882 0.240 6 31857051 downstream gene variant A/G snv 0.88 3
rs3095238 1.000 0.080 6 31193433 upstream gene variant T/G snv 0.88 1
rs2523485 1.000 0.080 6 31383258 upstream gene variant T/C snv 0.87 1
rs2530710 1.000 0.080 6 30972610 intergenic variant T/C snv 0.86 1
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 8
rs1323292
LOC105371664
0.882 0.160 1 192571891 intron variant G/A snv 0.86 1
rs3104373
HLA-DQA1
0.925 0.120 6 32632598 intron variant T/C snv 0.85 1