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
rs2068834
ZNF512
0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 9
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 7
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 6
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 5
rs2851682
FADS2
11 61848540 intron variant A/G snv 9.9E-02 5
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 5
rs10758593
GLIS3
0.827 0.240 9 4292083 intron variant G/A snv 0.45 4
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 4
rs13404446
TRIM54
0.925 0.120 2 27296386 intron variant G/A snv 0.42 4
rs1799884
GCK
1.000 0.080 7 44189469 intron variant C/T snv 0.17 4
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 4
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 4
rs4665965
MPV17
0.925 0.120 2 27313513 intron variant T/A;C snv 4
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 4
rs780110
IFT172
0.925 0.120 2 27462521 intron variant G/A snv 0.56 4
rs10814916
GLIS3
0.851 0.200 9 4293150 intron variant A/C snv 0.57 3
rs11605924
CRY2
1.000 0.080 11 45851540 intron variant A/C snv 0.39 3
rs11717195
ADCY5
1.000 0.080 3 123363551 intron variant T/C snv 0.19 3
rs11920090
SLC2A2
1.000 0.040 3 170999732 intron variant T/A snv 0.20 3
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 3
rs1371614
DPYSL5
2 26930006 intron variant C/T snv 0.29 3