Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 5
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 5
rs17817964
FTO
0.925 0.120 16 53794154 intron variant C/T snv 0.30 5
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 5
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 5
rs3794991
GATAD2A
1.000 0.080 19 19499787 intron variant C/G;T snv 7.4E-02 5
rs4430796
HNF1B
0.790 0.280 17 37738049 intron variant A/G snv 0.52 5
rs7202116
FTO
0.882 0.120 16 53787703 intron variant A/G snv 0.41 5
rs780092
GCKR
0.827 0.160 2 27520287 intron variant A/G snv 0.18 5
rs8176693
ABO
0.851 0.160 9 133262254 intron variant C/T snv 9.9E-02 5
rs910049
TSBP1-AS1 ; TSBP1
0.776 0.400 6 32347950 intron variant T/C snv 0.76 5
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 5
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 5
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 4
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs10758593
GLIS3
0.827 0.240 9 4292083 intron variant G/A snv 0.45 4
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 4
rs12056034
BAZ1B
0.882 0.160 7 73464315 intron variant A/G snv 9.2E-02 4
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 4
rs1799884
GCK
1.000 0.080 7 44189469 intron variant C/T snv 0.17 4
rs2000999
HPR ; TXNL4B
1.000 0.080 16 72074194 intron variant G/A snv 0.16 4
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 4
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 4
rs3751812
FTO
0.882 0.160 16 53784548 intron variant G/T snv 0.30 4
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 4