Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 23
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 22
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 20
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 20
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 18
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 18
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 17
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs11844632
RAD51B
0.708 0.280 14 68559662 intron variant G/A snv 0.23 17
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs2300206
RALY
0.708 0.280 20 34002002 intron variant G/C;T snv 17
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 17
rs11168936
TUBA1C
0.708 0.280 12 49251457 intron variant T/A;C snv 17
rs56404467
FRY
0.708 0.280 13 32265853 intron variant G/A snv 1.3E-02 17
rs481519
NEK10
0.708 0.280 3 27285723 intron variant C/A;T snv 17
rs115392158
HLA-B
0.708 0.280 6 31347004 intron variant A/G snv 17