Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9267673
C2 ; CYP21A2
0.925 0.080 6 31915902 intron variant C/A;T snv 0.12 4
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
rs34241101
SKIV2L ; CYP21A2
1.000 6 31968280 non coding transcript exon variant G/T snv 7.2E-02 8.7E-02 4