Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2420371
F5
1 169522317 intron variant G/A snv 0.95 4
rs1413885
DNAJC6
1 65349976 intron variant C/T snv 0.72 2
rs4133289
LINC02819
1 159484147 downstream gene variant C/T snv 0.16 2
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs2068834
ZNF512
0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 8
rs13022873
ZNF512
0.882 0.120 2 27592643 intron variant A/C;T snv 6
rs1919127
C2orf16
0.925 0.120 2 27578626 missense variant T/C snv 0.31 0.27 6
rs1919128
C2orf16
0.882 0.120 2 27578892 missense variant A/G snv 0.30 0.24 6
rs2911711 0.925 0.120 2 27527679 downstream gene variant T/A snv 0.58 6
rs3749147
GPN1 ; CCDC121
0.882 0.120 2 27629051 missense variant G/A snv 0.23 0.20 6
rs4666002
ZNF512
0.925 0.120 2 27617773 intron variant G/A;C snv 6
rs10208529
C2orf16
0.925 0.120 2 27563321 intron variant A/T snv 0.28 5
rs12467476
ZNF512
0.925 0.120 2 27602848 intron variant T/C snv 0.23 5
rs12478841
ZNF512
0.925 0.120 2 27588855 intron variant A/G snv 0.27 5
rs13002853
CCDC121 ; GPN1
0.925 0.120 2 27630378 intron variant C/G snv 0.20 5
rs2384656
ZNF512
0.925 0.120 2 27609188 intron variant A/G snv 0.27 5
rs4665382
C2orf16
0.925 0.120 2 27560934 intron variant T/C snv 0.23 5
rs4665383
C2orf16
0.925 0.120 2 27568688 synonymous variant C/G snv 0.24 5
rs4665987 0.925 0.120 2 27532958 upstream gene variant G/A;T snv 5
rs4665991
C2orf16
0.925 0.120 2 27543417 intron variant G/A snv 0.24 5
rs4666000
ZNF512
0.925 0.120 2 27616502 intron variant T/C snv 0.28 5
rs6760250
ZNF512
0.925 0.120 2 27589385 intron variant G/A;C snv 5