Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 12
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
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
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
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
rs1142
SRPK2
0.851 0.040 7 105115879 intron variant C/T snv 0.31 6
rs13101828
DGKQ
0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 6
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 6
rs7133378
DNAH10 ; CCDC92
12 123924955 intron variant G/A snv 0.38 6
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 5
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 5
rs2371767
ADAMTS9-AS2
3 64732582 intron variant G/C snv 0.38 5
rs2845885
FLRT1 ; MACROD1
11 64101590 intron variant C/T snv 0.87 5
rs3786897
PEPD
1.000 0.080 19 33402102 intron variant A/G snv 0.45 5
rs72959041
RSPO3
6 127133748 intron variant G/A snv 3.2E-02 5
rs7801581
HOXA11-AS ; HOXA11
7 27184152 intron variant C/T snv 0.24 5