Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 12
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
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
rs17145750
MLXIPL
0.925 0.120 7 73612048 intron variant C/A;T snv 7
rs12216125 0.925 0.120 6 25997230 intron variant C/T snv 0.26 6
rs2911711 0.925 0.120 2 27527679 downstream gene variant T/A snv 0.58 6
rs1178979
BAZ1B
0.925 0.120 7 73442100 3 prime UTR variant T/C snv 0.21 6
rs17145713
BAZ1B
0.925 0.120 7 73490480 intron variant C/T snv 0.21 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
rs3749147
GPN1 ; CCDC121
0.882 0.120 2 27629051 missense variant G/A snv 0.23 0.20 6
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 6
rs3887266
SLC17A3
0.925 0.120 6 25843518 intron variant C/T snv 8.9E-02 6
rs11974409
TBL2
0.925 0.120 7 73575060 intron variant A/G snv 0.16 6
rs13232120
TBL2
0.925 0.120 7 73568980 3 prime UTR variant A/T snv 0.11 6
rs17145738
TBL2
0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11 6
rs13022873
ZNF512
0.882 0.120 2 27592643 intron variant A/C;T snv 6
rs4666002
ZNF512
0.925 0.120 2 27617773 intron variant G/A;C snv 6
rs1150660 0.925 0.120 6 26101212 upstream gene variant A/C snv 0.73 5