Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 5
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 3
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 3
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 3
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 3
rs634869 6 139510620 intron variant T/A;C snv 2
rs11154370 6 126846446 intron variant A/G;T snv 1
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 1
rs11897119
MEIS1
2 66544868 intron variant T/A;C snv 1
rs12440667
LOXL1
1.000 0.040 15 73939098 intron variant C/A;T snv 1
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 1
rs1294421
LOC101928004
1.000 0.040 6 6742916 upstream gene variant T/A;C;G snv 1
rs1443512 12 53948900 downstream gene variant A/C;T snv 1
rs17568628 5 76751114 intergenic variant T/C;G snv 1
rs2119690 8 20002028 intergenic variant G/A;C snv 1
rs2145272 20 6645571 intergenic variant G/A;T snv 1
rs2820464
LYPLAL1-AS1
1 219519878 intergenic variant G/A;C snv 1
rs2894204
HLA-C
1.000 0.040 6 31269284 intron variant C/A;T snv 1
rs6701231
TBX15
1 118953038 intron variant C/A;G snv 1
rs6942652
CPED1
7 121249218 intron variant G/C;T snv 1
rs757608 17 61419916 regulatory region variant A/G;T snv 1
rs984222
TBX15
1 118961220 intron variant C/A;G snv 1