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
rs550605
C2 ; CYP21A2 ; C2-AS1
0.925 0.160 6 31939370 intron variant T/C snv 9.7E-02 0.12 2
rs9332739
CYP21A2 ; C2-AS1 ; C2
0.763 0.360 6 31936027 missense variant G/A;C snv 4.1E-06; 3.9E-02 2
rs609061
C2-AS1 ; C2 ; CYP21A2
1.000 0.120 6 31942385 intron variant G/A snv 0.12 1
rs497239
C2-AS1 ; CYP21A2 ; C2
1.000 0.120 6 31940984 intron variant T/C snv 0.12 1
rs9380272
C2-AS1 ; CYP21A2 ; C2
1.000 0.040 6 31938233 intron variant G/A snv 1
rs621701
CYP21A2 ; C2 ; C2-AS1
1.000 0.120 6 31935344 non coding transcript exon variant G/A snv 7.5E-02 1