Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs406936
CYP21A2 ; SKIV2L
0.882 0.240 6 31965384 intron variant G/A snv 0.19 3
rs437179
SKIV2L ; CYP21A2
0.882 0.160 6 31961237 missense variant A/C snv 0.76 0.78 3
rs492899
CYP21A2 ; SKIV2L
0.882 0.240 6 31965741 intron variant T/C snv 0.12 0.15 2
rs454212
SKIV2L ; CYP21A2
0.925 0.200 6 31966595 intron variant C/T snv 0.19 2
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
rs429608
CYP21A2 ; SKIV2L
0.851 0.160 6 31962685 intron variant G/A snv 0.14 0.16 1
rs419788
NELFE ; CYP21A2 ; SKIV2L
1.000 0.120 6 31961022 intron variant T/A;C snv 0.76 1
rs592229
SKIV2L ; CYP21A2
1.000 0.080 6 31962664 intron variant G/A;C;T snv 4.0E-06; 4.5E-05; 0.61 1