Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1809420
ADAMTS7
15 78764427 intron variant T/C snv 0.29 1
rs4833407
ALPK1
1.000 0.080 4 112390634 intron variant C/A;T snv 1
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 1
rs4923460
BDNF-AS ; LINC00678
11 27635242 intron variant G/T snv 0.20 1
rs700648
BOLL
2 197757912 intron variant C/T snv 0.50 1
rs4409766
BORCS7-ASMT ; BORCS7
1.000 0.040 10 102856906 intron variant T/C snv 0.14 1
rs11264483
C1orf61
1 156436589 intron variant G/C snv 0.45 1
rs12681792
CLVS1
8 61141904 intron variant C/A snv 0.23 1
rs10818854
DENND1A
0.851 0.200 9 123684499 intron variant G/A snv 5.7E-02 1
rs12899850
DENND4A ; RAB11A
15 65758961 intron variant C/T snv 0.19 1
rs7132908
FAIM2
1.000 0.080 12 49869365 3 prime UTR variant G/A snv 0.31 1
rs4947584
FIGNL1 ; DDC
1.000 0.120 7 50505011 intron variant A/T snv 0.35 1
rs9302652
FTO
1.000 0.080 16 53832063 intron variant C/T snv 0.74 1
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 1
rs7034200
GLIS3
1.000 0.080 9 4289050 intron variant C/A;G snv 1
rs7780752
GNGT1
7 93612328 intron variant T/C snv 0.27 1
rs10248619
GRB10
7 50683393 intron variant T/C snv 0.71 1
rs11658063
HNF1B
0.851 0.120 17 37743881 intron variant G/C;T snv 1
rs9299
HOXB5 ; HOXB3 ; HOXB-AS3
1.000 0.080 17 48592068 3 prime UTR variant C/A;T snv 1
rs4880341
JAKMIP3
10 132179185 intron variant C/T snv 0.54 1
rs6569648
L3MBTL3
1.000 0.080 6 130027974 intron variant C/T snv 0.84 1
rs11208659
LEPR
1.000 0.080 1 65513597 intron variant T/A;C snv 0.17 1
rs6048205
LINC00261
1.000 0.080 20 22578963 upstream gene variant A/G snv 9.1E-02 1
rs1412239
LINGO2
0.925 0.120 9 28425517 intron variant C/G snv 0.26 1
rs13179048
LOC101929710 ; MIR583HG
5 96207022 intron variant C/A snv 0.23 1