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
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 6
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 5
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 4
rs7193778 0.882 0.120 16 69529987 intergenic variant C/G;T snv 2
rs12982744
DOT1L
0.925 0.040 19 2177194 intron variant C/A;G;T snv 2
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 2
rs6976
GNL3 ; GLT8D1
0.851 0.080 3 52694788 3 prime UTR variant C/T snv 0.38 0.33 2
rs17050272
LOC105373585
0.882 0.120 2 120548864 upstream gene variant G/A snv 0.33 2
rs17786744
LOC107986931
0.882 0.120 8 23919493 intergenic variant A/G snv 0.37 2
rs1106766
R3HDM2
0.882 0.120 12 57415673 intron variant C/T snv 0.19 2
rs11177
SNORD136 ; GNL3 ; SNORD19 ; PBRM1
0.851 0.080 3 52687289 missense variant G/A snv 0.38 0.33 2
rs10947262
TSBP1-AS1 ; BTNL2
0.925 0.040 6 32405535 non coding transcript exon variant C/T snv 0.12 2
rs10492367 0.882 0.040 12 27862037 regulatory region variant G/T snv 0.12 1
rs182052
ADIPOQ
0.701 0.440 3 186842993 intron variant G/A snv 0.38 1
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 1
rs143383
GDF5
0.724 0.320 20 35438203 5 prime UTR variant G/A snv 0.47 1
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 1
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 1
rs3774354
ITIH1
0.882 0.080 3 52783659 intron variant G/A snv 0.31 1
rs3918242
MMP9
0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 1
rs10948172
SUPT3H ; LOC101929770
0.882 0.040 6 44809954 intron variant A/G snv 0.27 1