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
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 15
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 12
rs12953717
SMAD7
0.724 0.240 18 48927559 intron variant C/T snv 0.36 9
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 5
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs1800057
ATM
0.776 0.200 11 108272729 missense variant C/A;G snv 1.7E-02 4
rs718314
LOC105369705
0.882 0.120 12 26300350 intron variant A/G snv 0.27 4
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 3
rs74911261
POGLUT3
0.882 0.160 11 108486410 missense variant G/A snv 1.6E-02 1.6E-02 3
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 2
rs11894252
EPAS1
0.925 0.120 2 46306237 intron variant T/A;C;G snv 2
rs11263654 1.000 0.120 11 69423355 upstream gene variant C/T snv 0.11 1
rs11813268 0.925 0.120 10 103922538 upstream gene variant C/T snv 0.31 1
rs13376700 1.000 0.120 1 51011971 intergenic variant T/A snv 0.48 1
rs78971134 1.000 0.120 12 107258753 intergenic variant A/G snv 7.7E-02 1
rs182052
ADIPOQ
0.701 0.440 3 186842993 intron variant G/A snv 0.38 1
rs7913447
ANAPC16
1.000 0.120 10 72232282 intron variant C/A;T snv 1
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 1
rs3206824
DKK3
0.827 0.160 11 11964514 missense variant T/C snv 0.78 0.78 1
rs4903064
DPF3
0.925 0.120 14 72812712 intron variant T/C snv 0.23 1
rs11689011
EPAS1
1.000 0.120 2 46314037 intron variant T/A;C;G snv 1
rs2121266
EPAS1
1.000 0.120 2 46308785 intron variant C/A snv 0.61 1
rs4953345
EPAS1
1.000 0.120 2 46325462 intron variant T/A;C snv 1