Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11229
PRRC2A
0.851 0.280 6 31635993 synonymous variant A/G snv 0.14 0.17 6
rs1235162
GABBR1
0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs1265159
POU5F1
0.882 0.240 6 31172270 intron variant G/A snv 0.21 2
rs1270942
CFB ; CYP21A2
0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 6
rs1422673
TNIP1
0.925 0.160 5 151059427 intron variant C/G;T snv 2
rs1634718
MUC22
0.925 0.160 6 31005088 regulatory region variant A/G snv 0.20 2
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6
rs1980493
BTNL2 ; TSBP1-AS1
0.776 0.400 6 32395438 intron variant T/C snv 0.13 6
rs204990
GPSM3
0.851 0.280 6 32193653 intron variant C/A;T snv 4
rs2071591
ATP6V1G2-DDX39B ; ATP6V1G2 ; NFKBIL1
0.925 0.160 6 31548022 intron variant G/A;C snv 1
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs2233287
TNIP1
0.925 0.160 5 151060536 intron variant G/A snv 0.11 2
rs2233956
PSORS1C1 ; C6orf15
0.827 0.320 6 31113428 upstream gene variant T/C snv 0.12 3
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs2516400 0.827 0.320 6 31513328 upstream gene variant G/A snv 0.32 6
rs2517598
TRIM31 ; TRIM31-AS1
0.851 0.280 6 30112497 synonymous variant G/A snv 0.14 0.13 4
rs2523987
TRIM31-AS1 ; TRIM31
0.827 0.280 6 30112216 intron variant A/C snv 9.2E-02 5
rs2523989
TRIM31 ; TRIM31-AS1
0.827 0.280 6 30110498 missense variant C/T snv 0.12 0.12 4
rs2524005
HLA-A
0.882 0.160 6 29931900 upstream gene variant G/A snv 0.18 3
rs2596560 0.851 0.280 6 31387541 intergenic variant T/C snv 0.22 4
rs2844657 0.882 0.240 6 30861745 upstream gene variant A/G snv 0.17 3
rs2844659 0.851 0.280 6 30856755 intergenic variant C/G;T snv 4
rs2855812
MICB
0.790 0.360 6 31504943 intron variant G/T snv 0.23 6
rs2857595 0.827 0.320 6 31600692 intergenic variant G/A snv 0.27 6
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6