Source: GWASDB

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 1
rs6942652
CPED1
7 121249218 intron variant G/C;T snv 1
rs9931989
ATP2A1
16 28894763 intron variant G/C snv 0.68 3
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 1
rs7797307 7 69221140 intron variant G/C snv 7.6E-02 1
rs9647379
FNDC3B
3 172067378 intron variant G/C snv 0.32 1
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs2145272 20 6645571 intergenic variant G/A;T snv 1
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs2119690 8 20002028 intergenic variant G/A;C snv 1
rs2820464
LYPLAL1-AS1
1 219519878 intergenic variant G/A;C snv 1
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 6
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 6
rs12936587 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 3
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 3
rs9369425
LOC107986598
0.882 0.160 6 43843237 downstream gene variant G/A snv 0.66 3
rs12061508 1.000 0.040 1 196615338 intergenic variant G/A snv 0.23 2
rs1457489 1.000 0.080 18 60194728 upstream gene variant G/A snv 0.29 2
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 2
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 1
rs1020731
RBMS1
1.000 0.080 2 160287544 intron variant G/A snv 0.69 1
rs11724804
DGKQ
0.882 0.160 4 971991 intron variant G/A snv 0.43 1
rs12110693
LOC105377979
6 121837124 intergenic variant G/A snv 0.23 1
rs1254319
C14orf39
1.000 14 60437039 missense variant G/A snv 0.35 0.36 1