Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1178979
BAZ1B
0.925 0.120 7 73442100 3 prime UTR variant T/C snv 0.21 6
rs13022873
ZNF512
0.882 0.120 2 27592643 intron variant A/C;T snv 6
rs17145713
BAZ1B
0.925 0.120 7 73490480 intron variant C/T snv 0.21 6
rs2911711 0.925 0.120 2 27527679 downstream gene variant T/A snv 0.58 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
rs11983997 0.925 0.120 7 73524914 upstream gene variant G/A;C snv 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
rs6976930
BAZ1B
0.925 0.120 7 73471480 intron variant G/A snv 0.23 5
rs7811265
BAZ1B
0.925 0.120 7 73520180 intron variant A/G snv 0.23 5
rs13023094
SLC4A1AP
0.925 0.120 2 27687839 intron variant A/C snv 0.16 4
rs13030973
LINC01460
0.925 0.120 2 27705930 non coding transcript exon variant T/C snv 0.17 4