Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs389884
STK19 ; CYP21A2 ; DXO
0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 7
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 6
rs1980493
BTNL2 ; TSBP1-AS1
0.776 0.400 6 32395438 intron variant T/C snv 0.13 6
rs3130618
CSNK2B ; GPANK1
0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 6
rs652888
EHMT2-AS1 ; EHMT2 ; LOC107986588 ; CYP21A2
0.776 0.480 6 31883457 non coding transcript exon variant A/G snv 0.18 0.20 6
rs3132580
HCG21 ; SFTA2 ; MUCL3
0.790 0.360 6 30952347 missense variant G/A snv 8.0E-02 9.3E-02 6
rs3115663
PRRC2A ; MIR6832
0.827 0.360 6 31634066 non coding transcript exon variant T/C snv 0.17 6
rs7775397
TSBP1-AS1 ; TSBP1
0.790 0.400 6 32293475 missense variant T/G snv 6.0E-02 6.4E-02 6
rs3130564
PSORS1C1
0.790 0.360 6 31133897 intron variant C/T snv 0.14 5
rs7750641
TCF19
0.807 0.360 6 31161533 missense variant C/T snv 7.0E-02 7.6E-02 5
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 4
rs3129939
TSBP1-AS1 ; TSBP1
0.827 0.360 6 32368989 intron variant A/G snv 0.14 4
rs3134792
HLA-B
0.851 0.280 6 31344549 intron variant T/G snv 8.8E-02 3
rs2233956
PSORS1C1 ; C6orf15
0.827 0.320 6 31113428 upstream gene variant T/C snv 0.12 3
rs3134945
RNF5 ; MIR6833 ; AGPAT1
0.827 0.240 6 32178715 intron variant C/A snv 0.18 3
rs1265159
POU5F1
0.882 0.240 6 31172270 intron variant G/A snv 0.21 2
rs3096697
PPT2-EGFL8 ; PPT2 ; EGFL8
0.882 0.200 6 32166733 missense variant G/A snv 0.16 0.18 2
rs4664308
LOC105373717 ; PLA2R1
0.851 0.160 2 160060986 intron variant A/G snv 0.30 1