Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs644045
CYP21A2 ; C2
0.851 0.240 6 31916180 intron variant A/G snv 0.72 2
rs544167
CYP21A2 ; C2
0.925 0.160 6 31922381 intron variant T/G snv 7.3E-02 2
rs9332739
CYP21A2 ; C2-AS1 ; C2
0.763 0.360 6 31936027 missense variant G/A;C snv 4.1E-06; 3.9E-02 2
rs522162
CYP21A2 ; CFB ; NELFE
0.925 0.160 6 31952140 3 prime UTR variant T/C snv 0.12 2
rs387608
CYP21A2 ; DXO ; STK19
0.925 0.200 6 31973780 intron variant G/A snv 0.19 2
rs486416
CYP21A2 ; EHMT2
0.925 0.160 6 31888293 intron variant G/A snv 0.77 0.76 2
rs492899
CYP21A2 ; SKIV2L
0.882 0.240 6 31965741 intron variant T/C snv 0.12 0.15 2
rs2736428
CYP21A2 ; SLC44A4
0.925 0.160 6 31876147 intron variant C/T snv 0.33 0.26 2
rs550513
NELFE ; CYP21A2
0.925 0.160 6 31952910 intron variant C/T snv 0.12 2
rs454212
SKIV2L ; CYP21A2
0.925 0.200 6 31966595 intron variant C/T snv 0.19 2
rs438999
SKIV2L ; NELFE ; CYP21A2
0.925 0.160 6 31960529 missense variant A/G snv 9.7E-02 0.12 2
rs9267665
ZBTB12 ; C2 ; CYP21A2
0.925 0.200 6 31903079 intron variant C/T snv 7.3E-02 2
rs609061
C2-AS1 ; C2 ; CYP21A2
1.000 0.120 6 31942385 intron variant G/A snv 0.12 1
rs497239
C2-AS1 ; CYP21A2 ; C2
1.000 0.120 6 31940984 intron variant T/C snv 0.12 1
rs9380272
C2-AS1 ; CYP21A2 ; C2
1.000 0.040 6 31938233 intron variant G/A snv 1
rs2734335
C2 ; CYP21A2
1.000 0.120 6 31926167 intron variant G/A snv 0.53 1
rs641153
CFB ; CYP21A2
0.790 0.160 6 31946403 missense variant G/A;T snv 9.6E-02; 4.1E-06 1
rs511294
CYP21A2 ; C2
1.000 0.120 6 31921092 intron variant T/G snv 7.4E-02 1
rs498240
CYP21A2 ; C2
1.000 0.120 6 31924815 intron variant G/A snv 7.5E-02 1
rs497309
CYP21A2 ; C2
0.882 0.240 6 31924707 intron variant A/C;G snv 1
rs621701
CYP21A2 ; C2 ; C2-AS1
1.000 0.120 6 31935344 non coding transcript exon variant G/A snv 7.5E-02 1
rs537160
CYP21A2 ; CFB
0.882 0.240 6 31948623 intron variant A/G snv 0.73 1
rs12614
CYP21A2 ; CFB
0.851 0.160 6 31946402 missense variant C/G;T snv 4.1E-06; 0.12 1
rs760070
CYP21A2 ; CFB ; NELFE
0.882 0.280 6 31952179 3 prime UTR variant T/C snv 0.12 1
rs2243873
CYP21A2 ; EHMT2
1.000 0.080 6 31895656 non coding transcript exon variant C/A snv 0.61 1