Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7775759 0.925 0.200 6 31384669 upstream gene variant G/A snv 0.36 6
rs6933050 0.925 0.200 6 31375855 non coding transcript exon variant T/C snv 0.22 5
rs9266409 0.925 0.200 6 31368791 intron variant T/C snv 0.22 5
rs3818753
JAK1
1.000 0.200 1 64873549 3 prime UTR variant A/G snv 1.0E-02 3.6E-03 2
rs10236188 1.000 0.200 7 150548168 intergenic variant T/C snv 0.49 1
rs10256482 1.000 0.200 7 150653887 intergenic variant T/C snv 0.47 1
rs10277380 1.000 0.200 7 150533604 intergenic variant T/A;C snv 1
rs1522596 1.000 0.200 7 150538695 downstream gene variant A/G snv 0.47 1
rs1608157
LOC107986860
1.000 0.200 7 150549936 intergenic variant C/G;T snv 1
rs17006292
TFCP2L1
1.000 0.200 2 121261187 intron variant C/A snv 2.8E-02 1
rs1916012 1.000 0.200 7 150536739 intergenic variant A/G snv 0.49 1
rs1965673
WWC1
1.000 0.200 5 168411232 intron variant C/G snv 6.8E-02 1
rs2073716
CCHCR1
1.000 0.200 6 31155220 intron variant C/G snv 6.8E-02 1
rs2517411 1.000 0.200 6 30992490 downstream gene variant T/C;G snv 1
rs2617170
KLRC4 ; KLRC4-KLRK1
1.000 0.200 12 10408358 missense variant T/C snv 0.63 0.61 1
rs3093953
MICB
1.000 0.200 6 31506911 intron variant T/G snv 0.80 1
rs3094584
MICA
1.000 0.200 6 31416071 intron variant G/A;T snv 0.17 1
rs3095324
PSORS1C1 ; CDSN
1.000 0.200 6 31119356 intron variant C/T snv 0.35 1
rs386579334
CDSN ; PSORS1C1
1.000 0.200 6 31119356 intron variant C/T snv 1
rs4394274
HLA-B
1.000 0.200 6 31350387 intron variant C/A snv 0.40 1
rs6910516 1.000 0.200 6 31376050 non coding transcript exon variant A/C;G snv 1
rs7572482
STAT4
1.000 0.200 2 191150346 intron variant A/C;G snv 1
rs7574070
STAT4
1.000 0.200 2 191145762 intron variant A/C snv 0.55 1
rs9266406 1.000 0.200 6 31368641 intron variant G/A snv 0.22 1
rs9266490 1.000 0.200 6 31372381 intron variant A/G snv 0.22 1