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
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 20
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 9
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 9
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 8
rs1182188
GNA12
0.827 0.120 7 2830351 intron variant T/C snv 0.26 7
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs34517439
DNAJB4 ; GIPC2
0.882 0.120 1 77984833 intron variant C/A snv 7.3E-02 7
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 7
rs1142
SRPK2
0.851 0.040 7 105115879 intron variant C/T snv 0.31 6
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs7740107
L3MBTL3
1.000 0.080 6 130053316 intron variant T/A;G snv 6
rs10189857
BCL11A
1.000 0.080 2 60486100 intron variant A/G snv 0.42 5
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 5
rs114165349
LOC101928728 ; ARID1A
1 26695422 intron variant G/C snv 1.7E-02 5
rs16948048
ZNF652 ; LOC102724596
0.925 0.040 17 49363104 intron variant A/G snv 0.37 5
rs1812175
HHIP-AS1 ; HHIP
4 144653692 intron variant A/G snv 0.79 5
rs2812208
DLEU1
13 50132951 intron variant G/A;C snv 5
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 5
rs6569648
L3MBTL3
1.000 0.080 6 130027974 intron variant C/T snv 0.84 5
rs7141420
NRXN3
1.000 0.080 14 79433111 intron variant C/T snv 0.56 5
rs7801581
HOXA11-AS ; HOXA11
7 27184152 intron variant C/T snv 0.24 5
rs1635852
JAZF1
0.882 0.160 7 28149792 intron variant T/C snv 0.42 4
rs2247056
LOC112267902 ; HLA-B ; LINC02571
0.882 0.160 6 31297713 intron variant T/C snv 0.80 4
rs2282978
LOC112268009 ; CDK6
7 92635096 intron variant T/C snv 0.38 4