Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2072633
CFB ; CYP21A2 ; NELFE
0.807 0.320 6 31951801 3 prime UTR variant A/G snv 0.59 2
rs522162
CYP21A2 ; CFB ; NELFE
0.925 0.160 6 31952140 3 prime UTR variant T/C snv 0.12 2
rs550513
NELFE ; CYP21A2
0.925 0.160 6 31952910 intron variant C/T snv 0.12 2
rs438999
SKIV2L ; NELFE ; CYP21A2
0.925 0.160 6 31960529 missense variant A/G snv 9.7E-02 0.12 2
rs760070
CYP21A2 ; CFB ; NELFE
0.882 0.280 6 31952179 3 prime UTR variant T/C snv 0.12 1
rs403569
CYP21A2 ; MIR1236 ; NELFE
1.000 0.120 6 31957103 intron variant G/A snv 0.12 1
rs440454
CYP21A2 ; NELFE ; SKIV2L
1.000 0.120 6 31959565 non coding transcript exon variant A/G;T snv 1
rs419788
NELFE ; CYP21A2 ; SKIV2L
1.000 0.120 6 31961022 intron variant T/A;C snv 0.76 1