Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 9
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 8
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 7
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 6
rs11048456
LOC105369705
1.000 0.080 12 26310149 intron variant C/T snv 0.62 6
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs10184004 1.000 0.080 2 164651879 downstream gene variant C/T snv 0.48 5
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 5
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 5
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 5
rs3768321
PABPC4 ; PABPC4-AS1
1.000 0.080 1 39570256 intron variant G/T snv 0.14 5
rs3786897
PEPD
1.000 0.080 19 33402102 intron variant A/G snv 0.45 5
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 5
rs1169299
HNF1A
1.000 0.080 12 120991391 intron variant T/C snv 0.43 4
rs2296172
MACF1
1.000 0.080 1 39370145 missense variant A/G;T snv 0.19; 8.0E-06 4
rs2304130
ZNF101
1.000 0.080 19 19678719 splice region variant A/G snv 0.10 0.12 4
rs2972143 1.000 0.080 2 226251649 intergenic variant A/G snv 0.67 4
rs7144011
NRXN3
1.000 0.080 14 79474040 intron variant G/T snv 0.21 4
rs7570971
RAB3GAP1
1.000 0.080 2 135080336 intron variant C/A snv 0.61 4
rs9844972 1.000 0.080 3 150379848 regulatory region variant G/A;C snv 4
rs10011838 1.000 0.080 4 152599127 intergenic variant G/A snv 0.42 3
rs10734252 1.000 0.080 11 17383292 non coding transcript exon variant G/A snv 0.71 3
rs11066453
OAS1
1.000 0.080 12 112927816 intron variant A/G snv 3.8E-03 3
rs11558471
LOC105375716 ; SLC30A8
1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 3