Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1777672
NBEA
1.000 13 35603682 intron variant G/A snv 0.94 4
rs3094609
HCG27
0.925 0.080 6 31197789 non coding transcript exon variant T/C snv 0.86 0.89 5
rs2905722
MICB-DT
0.925 0.120 6 31481550 intron variant A/G snv 0.88 5
rs2523612
HLA-B
1.000 6 31353346 intron variant G/T snv 0.88 4
rs7381988
HLA-B
1.000 6 31278926 intron variant G/A snv 0.87 4
rs3132488
HLA-B
1.000 6 31274918 intron variant G/T snv 0.85 4
rs6457374
HLA-B ; LOC112267902
0.851 0.200 6 31304484 intron variant C/T snv 0.81 7
rs3130542 0.827 0.160 6 31264334 downstream gene variant A/G snv 0.81 5
rs2247056
LOC112267902 ; HLA-B ; LINC02571
0.882 0.160 6 31297713 intron variant T/C snv 0.80 8
rs3134899
MICB
1.000 6 31505509 intron variant C/T snv 0.80 4
rs2523578 1.000 6 31360765 upstream gene variant G/A snv 0.79 4
rs3132553
CDSN ; PSORS1C1
1.000 6 31117423 synonymous variant A/G snv 0.75 0.78 4
rs3132552
PSORS1C1 ; CDSN
1.000 6 31117492 synonymous variant A/G snv 0.76 0.78 4
rs3132546
PSORS1C1 ; CDSN
1.000 6 31120802 intron variant A/G snv 0.78 4
rs3130984
CDSN ; PSORS1C1
1.000 6 31117187 missense variant T/C snv 0.76; 4.0E-06 0.78 4
rs3130558
PSORS1C1
0.925 0.080 6 31129406 intron variant C/G snv 0.77 5
rs12122100
LOC728989 ; NBPF13P
1.000 1 147037378 intron variant T/C snv 0.76 4
rs2239519
PSORS1C1 ; CDSN
1.000 6 31121079 intron variant T/C snv 0.76 4
rs3132545
PSORS1C1 ; CDSN
1.000 6 31121348 intron variant A/G snv 0.76 4
rs3131034
DDR1
0.925 0.080 6 30886019 intron variant G/A snv 0.75 5
rs2517459 0.882 0.160 6 30929245 downstream gene variant T/C snv 0.74 5
rs2523554 0.925 0.080 6 31364052 upstream gene variant C/T snv 0.70 5
rs6906846
HLA-B ; USP8P1
0.851 0.280 6 31277959 non coding transcript exon variant A/G snv 0.67 6
rs2596531 1.000 6 31419780 intron variant C/T snv 0.64 4
rs3094204
PSORS1C1
1.000 6 31124215 intron variant A/G snv 0.61 4