Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs437179
SKIV2L ; CYP21A2
0.882 0.160 6 31961237 missense variant A/C snv 0.76 0.78 3
rs630379
NELFE ; CYP21A2
0.882 0.200 6 31954477 intron variant A/C snv 0.77 0.79 3
rs497309
CYP21A2 ; C2
0.882 0.240 6 31924707 intron variant A/C;G snv 1
rs389884
STK19 ; CYP21A2 ; DXO
0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 7
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
rs1270942
CFB ; CYP21A2
0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 6
rs2072633
CFB ; CYP21A2 ; NELFE
0.807 0.320 6 31951801 3 prime UTR variant A/G snv 0.59 2
rs644045
CYP21A2 ; C2
0.851 0.240 6 31916180 intron variant A/G snv 0.72 2
rs438999
SKIV2L ; NELFE ; CYP21A2
0.925 0.160 6 31960529 missense variant A/G snv 9.7E-02 0.12 2
rs537160
CYP21A2 ; CFB
0.882 0.240 6 31948623 intron variant A/G snv 0.73 1
rs6907185
CYP21A2 ; SLC44A4
1.000 0.120 6 31876907 intron variant A/G snv 8.9E-02 1
rs440454
CYP21A2 ; NELFE ; SKIV2L
1.000 0.120 6 31959565 non coding transcript exon variant A/G;T snv 1
rs605203
EHMT2-AS1 ; LOC107986588 ; CYP21A2 ; SLC44A4
1.000 0.120 6 31879235 intron variant C/A snv 0.77 1
rs2243873
CYP21A2 ; EHMT2
1.000 0.080 6 31895656 non coding transcript exon variant C/A snv 0.61 1
rs660550
SLC44A4 ; CYP21A2
0.882 0.160 6 31869500 intron variant C/A;G snv 0.60 3
rs9267673
C2 ; CYP21A2
0.925 0.080 6 31915902 intron variant C/A;T snv 0.12 4
rs12614
CYP21A2 ; CFB
0.851 0.160 6 31946402 missense variant C/G;T snv 4.1E-06; 0.12 1
rs4151664
CYP21A2 ; NELFE
1.000 6 31953096 intron variant C/T snv 8.7E-02 4
rs2242665
CYP21A2 ; SLC44A4
0.882 0.160 6 31871532 missense variant C/T snv 0.60 0.60 3
rs454212
SKIV2L ; CYP21A2
0.925 0.200 6 31966595 intron variant C/T snv 0.19 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
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
rs11966200
SLC44A4 ; CYP21A2
0.851 0.040 6 31869289 intron variant C/T snv 2.9E-02 4.5E-02 1