Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 16
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 13
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 10
rs11205303
MTMR11
0.882 0.120 1 149934520 missense variant T/C snv 0.33 0.29 9
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 7
rs7133378
DNAH10 ; CCDC92
12 123924955 intron variant G/A snv 0.38 6
rs55872725
FTO
16 53775211 intron variant C/T snv 0.31 6
rs2274224
PLCE1-AS1 ; PLCE1
0.882 0.080 10 94279840 missense variant G/A;C snv 8.8E-05; 0.44 6
rs62033406
FTO
16 53790314 intron variant A/G snv 0.33 5
rs12140153
PATJ
1 62114219 missense variant G/A;T snv 4.0E-06; 5.9E-02 5
rs62104180 2 466003 intergenic variant G/A snv 2.9E-02 4
rs6545714 2 59080590 intron variant G/A;C snv 4
rs3749237
IP6K1
3 49732599 intron variant G/A snv 0.26 4
rs900399
LINC02029
3 157080943 upstream gene variant A/G snv 0.36 4
rs6755502 2 635721 intergenic variant T/C snv 0.85 3
rs879620
ADCY9
16 3965728 3 prime UTR variant C/T snv 0.49 0.46 3
rs71658797
AK5
0.925 0.080 1 77501822 intron variant T/A snv 7.3E-02 3
rs1591805
CENPW
1.000 0.040 6 126395918 intron variant A/G snv 0.47 3
rs757318
CRTC1
19 18709498 intron variant C/A;G;T snv 3
rs9906944
IGF2BP1
17 49014058 intron variant C/G;T snv 3