Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs558702
C2 ; ZBTB12 ; CYP21A2
0.807 0.320 6 31902549 intron variant G/A snv 7.7E-02 6
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
rs9267673
C2 ; CYP21A2
0.925 0.080 6 31915902 intron variant C/A;T snv 0.12 4
rs659445
EHMT2 ; CYP21A2 ; C2
0.882 0.160 6 31896527 intron variant G/A;C snv 0.77 0.76 3
rs6941112
CYP21A2 ; STK19
0.882 0.120 6 31978837 intron variant G/A snv 0.25 3
rs660550
SLC44A4 ; CYP21A2
0.882 0.160 6 31869500 intron variant C/A;G snv 0.60 3
rs406936
CYP21A2 ; SKIV2L
0.882 0.240 6 31965384 intron variant G/A snv 0.19 3
rs9267658
CYP21A2 ; SLC44A4 ; EHMT2-AS1
0.882 0.240 6 31878208 intron variant T/C snv 0.91 3
rs630379
NELFE ; CYP21A2
0.882 0.200 6 31954477 intron variant A/C snv 0.77 0.79 3
rs486416
CYP21A2 ; EHMT2
0.925 0.160 6 31888293 intron variant G/A snv 0.77 0.76 2
rs454212
SKIV2L ; CYP21A2
0.925 0.200 6 31966595 intron variant C/T snv 0.19 2
rs644045
CYP21A2 ; C2
0.851 0.240 6 31916180 intron variant A/G snv 0.72 2
rs550605
C2 ; CYP21A2 ; C2-AS1
0.925 0.160 6 31939370 intron variant T/C snv 9.7E-02 0.12 2
rs2736428
CYP21A2 ; SLC44A4
0.925 0.160 6 31876147 intron variant C/T snv 0.33 0.26 2
rs387608
CYP21A2 ; DXO ; STK19
0.925 0.200 6 31973780 intron variant G/A snv 0.19 2
rs550513
NELFE ; CYP21A2
0.925 0.160 6 31952910 intron variant C/T snv 0.12 2
rs544167
CYP21A2 ; C2
0.925 0.160 6 31922381 intron variant T/G snv 7.3E-02 2
rs492899
CYP21A2 ; SKIV2L
0.882 0.240 6 31965741 intron variant T/C snv 0.12 0.15 2
rs9267665
ZBTB12 ; C2 ; CYP21A2
0.925 0.200 6 31903079 intron variant C/T snv 7.3E-02 2
rs7743807
EHMT2 ; CYP21A2
1.000 0.120 6 31886766 intron variant C/T snv 2.9E-02 5.2E-02 1
rs537160
CYP21A2 ; CFB
0.882 0.240 6 31948623 intron variant A/G snv 0.73 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