Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042663
C2 ; CYP21A2 ; C2-AS1
0.925 0.160 6 31937353 synonymous variant G/A snv 9.7E-02 0.12 2
rs11966200
SLC44A4 ; CYP21A2
0.851 0.040 6 31869289 intron variant C/T snv 2.9E-02 4.5E-02 1
rs12614
CYP21A2 ; CFB
0.851 0.160 6 31946402 missense variant C/G;T snv 4.1E-06; 0.12 1
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
rs2242665
CYP21A2 ; SLC44A4
0.882 0.160 6 31871532 missense variant C/T snv 0.60 0.60 3
rs2243873
CYP21A2 ; EHMT2
1.000 0.080 6 31895656 non coding transcript exon variant C/A snv 0.61 1
rs2734335
C2 ; CYP21A2
1.000 0.120 6 31926167 intron variant G/A snv 0.53 1
rs2736428
CYP21A2 ; SLC44A4
0.925 0.160 6 31876147 intron variant C/T snv 0.33 0.26 2
rs34241101
SKIV2L ; CYP21A2
1.000 6 31968280 non coding transcript exon variant G/T snv 7.2E-02 8.7E-02 4
rs387608
CYP21A2 ; DXO ; STK19
0.925 0.200 6 31973780 intron variant G/A snv 0.19 2
rs389512
CYP21A2 ; STK19
1.000 0.120 6 31979817 non coding transcript exon variant G/A;C snv 1
rs389883
CYP21A2 ; STK19
0.827 0.200 6 31979683 non coding transcript exon variant G/T snv 0.80 4
rs389884
STK19 ; CYP21A2 ; DXO
0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 7
rs401775
CYP21A2 ; SKIV2L
1.000 6 31963360 intron variant T/C snv 0.23 4
rs403569
CYP21A2 ; MIR1236 ; NELFE
1.000 0.120 6 31957103 intron variant G/A snv 0.12 1
rs406936
CYP21A2 ; SKIV2L
0.882 0.240 6 31965384 intron variant G/A snv 0.19 3
rs4151657
CFB ; CYP21A2
0.925 0.160 6 31949763 non coding transcript exon variant T/C snv 0.27 2
rs4151664
CYP21A2 ; NELFE
1.000 6 31953096 intron variant C/T snv 8.7E-02 4
rs419788
NELFE ; CYP21A2 ; SKIV2L
1.000 0.120 6 31961022 intron variant T/A;C snv 0.76 1
rs429608
CYP21A2 ; SKIV2L
0.851 0.160 6 31962685 intron variant G/A snv 0.14 0.16 1
rs437179
SKIV2L ; CYP21A2
0.882 0.160 6 31961237 missense variant A/C snv 0.76 0.78 3
rs438999
SKIV2L ; NELFE ; CYP21A2
0.925 0.160 6 31960529 missense variant A/G snv 9.7E-02 0.12 2
rs440454
CYP21A2 ; NELFE ; SKIV2L
1.000 0.120 6 31959565 non coding transcript exon variant A/G;T snv 1
rs454212
SKIV2L ; CYP21A2
0.925 0.200 6 31966595 intron variant C/T snv 0.19 2