Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
rs1235162
GABBR1
0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 6
rs3132580
HCG21 ; SFTA2 ; MUCL3
0.790 0.360 6 30952347 missense variant G/A snv 8.0E-02 9.3E-02 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
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 6
rs660895
HLA-DRB1
0.752 0.360 6 32609603 intergenic variant A/G snv 0.19 6
rs2534657
MICB
0.882 0.200 6 31504682 intron variant C/T snv 0.15 6
rs2855812
MICB
0.790 0.360 6 31504943 intron variant G/T snv 0.23 6
rs3131379
MSH5 ; MSH5-SAPCD1
0.752 0.440 6 31753256 intron variant G/A snv 6.4E-02 7.9E-02 6
rs3131296
NOTCH4
0.807 0.320 6 32205216 intron variant C/T snv 0.11 6
rs3134942
NOTCH4
0.790 0.320 6 32200994 synonymous variant G/T snv 9.7E-02 0.11 6
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs11229
PRRC2A
0.851 0.280 6 31635993 synonymous variant A/G snv 0.14 0.17 6
rs2260000
PRRC2A
0.851 0.200 6 31625699 intron variant A/G snv 0.29 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