Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 16
rs10131032
AKAP6
1.000 0.040 14 32780875 intron variant G/A snv 9.3E-02 2
rs10506868
VTI1A
0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 9
rs1058319
SLC2A4RG
1.000 0.040 20 63743036 3 prime UTR variant C/A;T snv 0.21 1
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 6
rs1063192
CDKN2B ; CDKN2B-AS1
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 3
rs10842893
STK38L
1.000 0.040 12 27269953 intron variant C/T snv 7.1E-02 1
rs10852606
HEATR3
0.882 0.040 16 50094961 intron variant T/A;C snv 4
rs10892258
LOC105369519
0.925 0.120 11 118709156 intron variant G/A snv 0.19 1
rs11079041
STAT5B
0.882 0.040 17 42262061 intron variant T/A;C snv 0.36 1
rs111696067
GOLGA3
1.000 0.040 12 132799954 intron variant T/C snv 5.3E-04 2
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13 9
rs11216930
PHLDB1
1.000 0.040 11 118618067 intron variant A/C snv 0.22 1
rs11233250
MIR4300HG
0.882 0.040 11 82685972 intron variant C/T snv 0.11 4
rs11598018
STN1
1.000 0.040 10 103901557 intron variant C/A;T snv 2
rs11599775
VTI1A
1.000 0.040 10 112699938 intron variant G/A snv 0.27 2
rs11603023
PHLDB1
0.925 0.120 11 118615352 intron variant T/C snv 0.57 1
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 1
rs11706832
LRIG1
1.000 0.040 3 66452557 intron variant A/C;G snv 2
rs11979158
EGFR
0.882 0.040 7 55091656 intron variant A/G;T snv 0.20 4
rs12076373
AKT3
1.000 0.040 1 243688645 intron variant G/C snv 0.20 2
rs12230172
LOC105369844
0.882 0.040 12 75848895 intron variant A/G snv 0.48 2
rs12241008
VTI1A
0.716 0.160 10 112520943 intron variant T/C snv 0.13 9
rs12752552
RAVER2
0.882 0.040 1 64763616 intron variant T/C snv 0.13 4
rs1275600
LOC105369844
1.000 0.040 12 75869771 intron variant T/A snv 0.47 2