Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 13
rs998584 6 43790159 downstream gene variant C/A snv 0.41 10
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 9
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 9
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 9
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 8
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 8
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 8
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs11694173
THADA
0.827 0.080 2 43363760 intron variant G/A snv 0.14 7
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 7
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 7
rs2145272 20 6645571 intergenic variant G/A;T snv 7
rs2283847
MN1
22 27785411 intron variant C/A;G;T snv 7
rs863750
ZNF664-RFLNA ; RFLNA
12 124020897 intron variant C/T snv 0.53 7
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 6
rs10808546 8 125483576 intron variant C/T snv 0.39 6