Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4151664
CYP21A2 ; NELFE
1.000 6 31953096 intron variant C/T snv 8.7E-02 4
rs401775
CYP21A2 ; SKIV2L
1.000 6 31963360 intron variant T/C snv 0.23 4
rs34241101
SKIV2L ; CYP21A2
1.000 6 31968280 non coding transcript exon variant G/T snv 7.2E-02 8.7E-02 4
rs9267655
CYP21A2 ; SLC44A4
1.000 0.040 6 31873278 intron variant G/A snv 0.16 1
rs11966200
SLC44A4 ; CYP21A2
0.851 0.040 6 31869289 intron variant C/T snv 2.9E-02 4.5E-02 1
rs9380272
C2-AS1 ; CYP21A2 ; C2
1.000 0.040 6 31938233 intron variant G/A snv 1
rs9267673
C2 ; CYP21A2
0.925 0.080 6 31915902 intron variant C/A;T snv 0.12 4
rs2243873
CYP21A2 ; EHMT2
1.000 0.080 6 31895656 non coding transcript exon variant C/A snv 0.61 1
rs592229
SKIV2L ; CYP21A2
1.000 0.080 6 31962664 intron variant G/A;C;T snv 4.0E-06; 4.5E-05; 0.61 1
rs6941112
CYP21A2 ; STK19
0.882 0.120 6 31978837 intron variant G/A snv 0.25 3
rs494620
SLC44A4 ; CYP21A2
0.925 0.120 6 31870936 stop gained G/A;T snv 0.44; 4.1E-06 3
rs7743807
EHMT2 ; CYP21A2
1.000 0.120 6 31886766 intron variant C/T snv 2.9E-02 5.2E-02 1
rs589428
SLC44A4 ; CYP21A2 ; EHMT2 ; LOC107986588 ; EHMT2-AS1
1.000 0.120 6 31880443 non coding transcript exon variant T/G snv 0.77 1
rs440454
CYP21A2 ; NELFE ; SKIV2L
1.000 0.120 6 31959565 non coding transcript exon variant A/G;T snv 1
rs403569
CYP21A2 ; MIR1236 ; NELFE
1.000 0.120 6 31957103 intron variant G/A snv 0.12 1
rs419788
NELFE ; CYP21A2 ; SKIV2L
1.000 0.120 6 31961022 intron variant T/A;C snv 0.76 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
rs2734335
C2 ; CYP21A2
1.000 0.120 6 31926167 intron variant G/A snv 0.53 1
rs621701
CYP21A2 ; C2 ; C2-AS1
1.000 0.120 6 31935344 non coding transcript exon variant G/A snv 7.5E-02 1
rs6907185
CYP21A2 ; SLC44A4
1.000 0.120 6 31876907 intron variant A/G snv 8.9E-02 1
rs605203
EHMT2-AS1 ; LOC107986588 ; CYP21A2 ; SLC44A4
1.000 0.120 6 31879235 intron variant C/A snv 0.77 1
rs389512
CYP21A2 ; STK19
1.000 0.120 6 31979817 non coding transcript exon variant G/A;C snv 1
rs497239
C2-AS1 ; CYP21A2 ; C2
1.000 0.120 6 31940984 intron variant T/C snv 0.12 1
rs609061
C2-AS1 ; C2 ; CYP21A2
1.000 0.120 6 31942385 intron variant G/A snv 0.12 1