Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9267658
CYP21A2 ; SLC44A4 ; EHMT2-AS1
0.882 0.240 6 31878208 intron variant T/C snv 0.91 3
rs389883
CYP21A2 ; STK19
0.827 0.200 6 31979683 non coding transcript exon variant G/T snv 0.80 4
rs630379
NELFE ; CYP21A2
0.882 0.200 6 31954477 intron variant A/C snv 0.77 0.79 3
rs437179
SKIV2L ; CYP21A2
0.882 0.160 6 31961237 missense variant A/C snv 0.76 0.78 3
rs589428
SLC44A4 ; CYP21A2 ; EHMT2 ; LOC107986588 ; EHMT2-AS1
1.000 0.120 6 31880443 non coding transcript exon variant T/G snv 0.77 1
rs605203
EHMT2-AS1 ; LOC107986588 ; CYP21A2 ; SLC44A4
1.000 0.120 6 31879235 intron variant C/A snv 0.77 1
rs659445
EHMT2 ; CYP21A2 ; C2
0.882 0.160 6 31896527 intron variant G/A;C snv 0.77 0.76 3
rs486416
CYP21A2 ; EHMT2
0.925 0.160 6 31888293 intron variant G/A snv 0.77 0.76 2
rs537160
CYP21A2 ; CFB
0.882 0.240 6 31948623 intron variant A/G snv 0.73 1
rs644045
CYP21A2 ; C2
0.851 0.240 6 31916180 intron variant A/G snv 0.72 2
rs2243873
CYP21A2 ; EHMT2
1.000 0.080 6 31895656 non coding transcript exon variant C/A snv 0.61 1
rs644827
SLC44A4 ; CYP21A2
0.882 0.160 6 31870664 missense variant T/C snv 0.60 0.60 3
rs2242665
CYP21A2 ; SLC44A4
0.882 0.160 6 31871532 missense variant C/T snv 0.60 0.60 3
rs2072633
CFB ; CYP21A2 ; NELFE
0.807 0.320 6 31951801 3 prime UTR variant A/G snv 0.59 2
rs2734335
C2 ; CYP21A2
1.000 0.120 6 31926167 intron variant G/A snv 0.53 1
rs4151657
CFB ; CYP21A2
0.925 0.160 6 31949763 non coding transcript exon variant T/C snv 0.27 2
rs2736428
CYP21A2 ; SLC44A4
0.925 0.160 6 31876147 intron variant C/T snv 0.33 0.26 2
rs6941112
CYP21A2 ; STK19
0.882 0.120 6 31978837 intron variant G/A snv 0.25 3
rs401775
CYP21A2 ; SKIV2L
1.000 6 31963360 intron variant T/C snv 0.23 4
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
rs387608
CYP21A2 ; DXO ; STK19
0.925 0.200 6 31973780 intron variant G/A snv 0.19 2
rs454212
SKIV2L ; CYP21A2
0.925 0.200 6 31966595 intron variant C/T snv 0.19 2
rs406936
CYP21A2 ; SKIV2L
0.882 0.240 6 31965384 intron variant G/A snv 0.19 3
rs9267655
CYP21A2 ; SLC44A4
1.000 0.040 6 31873278 intron variant G/A snv 0.16 1
rs429608
CYP21A2 ; SKIV2L
0.851 0.160 6 31962685 intron variant G/A snv 0.14 0.16 1