Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2844511 0.807 0.200 6 31422007 intron variant A/G;T snv 7
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs3815087
PSORS1C1
0.851 0.200 6 31125810 5 prime UTR variant G/A snv 0.25 7
rs389884
STK19 ; CYP21A2 ; DXO
0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 7
rs6457374
HLA-B ; LOC112267902
0.851 0.200 6 31304484 intron variant C/T snv 0.81 7
rs11229
PRRC2A
0.851 0.280 6 31635993 synonymous variant A/G snv 0.14 0.17 6
rs1270942
CFB ; CYP21A2
0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 6
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
rs2156875
HLA-B
0.882 0.200 6 31349570 intron variant C/T snv 0.50 6
rs2260000
PRRC2A
0.851 0.200 6 31625699 intron variant A/G snv 0.29 6
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 6
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs2736172
PRRC2A ; SNORA38
0.882 0.160 6 31623121 non coding transcript exon variant C/T snv 0.41 0.29 6
rs2844509
SNORD84 ; DDX39B-AS1 ; DDX39B ; ATP6V1G2-DDX39B
0.882 0.160 6 31543147 intron variant A/G snv 0.23 6
rs2844513 0.925 0.120 6 31420437 intron variant G/A snv 0.53 6
rs2855812
MICB
0.790 0.360 6 31504943 intron variant G/T snv 0.23 6
rs2856997
HLA-DOB
0.882 0.200 6 32813999 non coding transcript exon variant C/A snv 0.45 6
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 6
rs3115663
PRRC2A ; MIR6832
0.827 0.360 6 31634066 non coding transcript exon variant T/C snv 0.17 6
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 6
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 6
rs3130618
CSNK2B ; GPANK1
0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 6
rs3131296
NOTCH4
0.807 0.320 6 32205216 intron variant C/T snv 0.11 6