Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6
rs2516400 0.827 0.320 6 31513328 upstream gene variant G/A snv 0.32 6
rs2857595 0.827 0.320 6 31600692 intergenic variant G/A snv 0.27 6
rs3130473 0.882 0.160 6 31231431 intergenic variant C/T snv 0.23 6
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 6
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 5
rs3129890 0.827 0.280 6 32446496 downstream gene variant T/A;C snv 5
rs3130350 0.827 0.280 6 30360062 upstream gene variant G/T snv 7.1E-02 5
rs2596560 0.851 0.280 6 31387541 intergenic variant T/C snv 0.22 4
rs2844659 0.851 0.280 6 30856755 intergenic variant C/G;T snv 4
rs3129963 0.851 0.280 6 32412431 downstream gene variant A/G snv 0.17 4
rs2844657 0.882 0.240 6 30861745 upstream gene variant A/G snv 0.17 3
rs3095089 0.882 0.240 6 30966017 upstream gene variant G/T snv 0.16 3
rs3135353 0.882 0.280 6 32425100 intergenic variant C/T snv 9.4E-02 3
rs7749323 0.925 0.200 6 137909252 intergenic variant G/A snv 3.3E-02 1
rs3132610
ABCF1
0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 5
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs2071591
ATP6V1G2-DDX39B ; ATP6V1G2 ; NFKBIL1
0.925 0.160 6 31548022 intron variant G/A;C snv 1
rs1980493
BTNL2 ; TSBP1-AS1
0.776 0.400 6 32395438 intron variant T/C snv 0.13 6
rs558702
C2 ; ZBTB12 ; CYP21A2
0.807 0.320 6 31902549 intron variant G/A snv 7.7E-02 6
rs1270942
CFB ; CYP21A2
0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 6
rs3130618
CSNK2B ; GPANK1
0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 6
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs1235162
GABBR1
0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6