Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9889895 17 34495359 intergenic variant G/A snv 0.12 1
rs9663362
PLCE1
10 94135420 intron variant G/A;C snv 1
rs9590141 13 94951368 intergenic variant G/A snv 8.4E-02 1
rs943580 1 230701298 upstream gene variant G/A snv 0.42 1
rs9399401
ADGRG6
1.000 0.040 6 142347764 intron variant T/C snv 0.31 2
rs932764
PLCE1
10 94136183 intron variant A/G snv 0.38 4
rs9313772
LINC02227
5 158377449 intron variant C/T snv 0.30 1
rs9296832
COL21A1
6 56236111 intron variant C/G snv 0.56 1
rs9290370
MECOM
3 169607225 intron variant T/G snv 0.78 1
rs880315
CASZ1
0.925 0.120 1 10736809 intron variant T/C snv 0.32 1
rs871606 4 53933078 intron variant T/C;G snv 1
rs825937 2 4760437 intergenic variant C/A;T snv 1
rs8087081 18 62679966 intergenic variant T/A snv 8.5E-02 1
rs8069437
LRRC37A2 ; WNT3
17 46829583 intron variant T/C snv 0.82 1
rs7984522
MYO16
13 108695311 intron variant T/A;C snv 1
rs7951100 11 55822820 upstream gene variant G/T snv 4.5E-02 1
rs7943453
OR8I2
11 56091949 upstream gene variant G/A snv 6.0E-02 1
rs7936086 11 55923383 intergenic variant C/A;T snv 1
rs7935728 11 56111979 downstream gene variant C/T snv 6.0E-02 1
rs7929570 11 56109777 downstream gene variant T/C snv 6.0E-02 1
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs7733088
HTR4 ; LOC107986462
1.000 0.040 5 148476770 intron variant G/A;C snv 0.44; 4.1E-06 3
rs7726475
SUB1
5 32575808 intron variant G/A;C snv 1
rs7655625 1.000 0.040 4 144564763 intron variant T/C;G snv 2
rs7591163 2 227850659 intergenic variant C/A;G;T snv 1