Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3130473 0.882 0.160 6 31231431 intergenic variant C/T snv 0.23 6
rs7775759 0.925 0.200 6 31384669 upstream gene variant G/A snv 0.36 6
rs2284178
HCP5
0.925 0.120 6 31464348 non coding transcript exon variant C/T snv 0.44 6
rs2156875
HLA-B
0.882 0.200 6 31349570 intron variant C/T snv 0.50 6
rs6906846
HLA-B ; USP8P1
0.851 0.280 6 31277959 non coding transcript exon variant A/G snv 0.67 6
rs2856997
HLA-DOB
0.882 0.200 6 32813999 non coding transcript exon variant C/A snv 0.45 6
rs2894207
LINC02571 ; HLA-B
0.882 0.160 6 31295974 intron variant T/C snv 0.20 6
rs9366778
LINC02571 ; LOC112267902 ; HLA-B
0.925 0.120 6 31301396 intron variant G/A snv 0.47 6
rs9264942
LOC112267902 ; HLA-B
0.763 0.400 6 31306603 intron variant T/C snv 0.34 6
rs2534657
MICB
0.882 0.200 6 31504682 intron variant C/T snv 0.15 6
rs2260000
PRRC2A
0.851 0.200 6 31625699 intron variant A/G snv 0.29 6
rs2736172
PRRC2A ; SNORA38
0.882 0.160 6 31623121 non coding transcript exon variant C/T snv 0.41 0.29 6
rs3823418
PSORS1C1
0.925 0.120 6 31133165 intron variant G/A snv 0.23 6
rs527476195
PSORS1C1
0.925 0.120 6 31133165 intron variant G/A snv 6
rs2844509
SNORD84 ; DDX39B-AS1 ; DDX39B ; ATP6V1G2-DDX39B
0.882 0.160 6 31543147 intron variant A/G snv 0.23 6
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 6
rs9391858
TSBP1-AS1 ; TSBP1
0.925 0.080 6 32373621 intron variant A/G snv 0.13 6
rs6906662
TSBP1 ; TSBP1-AS1
0.882 0.200 6 32298729 intron variant G/A snv 6.8E-02 6
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 6
rs259919
ZNRD1ASP
0.882 0.080 6 30057726 intron variant G/A snv 0.25 6
rs10947207 1.000 6 31393708 downstream gene variant T/C snv 0.31 5
rs13211318 0.925 0.040 6 32134903 upstream gene variant A/C snv 0.11 5
rs13437088 0.925 0.040 6 31387342 intergenic variant C/T snv 0.32 5
rs17475879 0.925 0.040 6 30396731 regulatory region variant C/T snv 5.6E-02 5
rs2219893 0.925 0.120 6 32801886 intergenic variant T/C snv 0.33 5