Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12149832
FTO
0.851 0.120 16 53808996 intron variant G/A snv 0.31 3
rs12579350
ANO2
0.882 0.080 12 5687935 intron variant G/A snv 0.12 3
rs1392817
PDE4B
0.925 0.040 1 66073773 intron variant A/G snv 0.51 3
rs17694493
CDKN2B-AS1
0.882 0.120 9 22041999 intron variant C/G snv 0.12 3
rs1828853
MIR4300HG
0.925 0.040 11 82371520 intron variant G/A;C;T snv 3
rs2145839
LOC105372648
0.925 0.040 20 48856501 regulatory region variant G/T snv 0.29 3
rs41520844
WRN
0.882 0.080 8 31135670 intron variant A/T snv 7.1E-02 3
rs4364959
DNAJC1
0.882 0.080 10 21996442 intron variant C/T snv 0.77 3
rs6871087 0.925 0.040 5 30899410 intergenic variant A/G snv 8.5E-02 3
rs7090135
RPS24
0.882 0.080 10 78043832 intron variant G/A;C snv 0.13 3
rs739496
SH2B3 ; ATXN2
0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27 3
rs7741741
ADGRG6
0.925 0.040 6 142334664 intron variant T/A;G snv 3
rs886448
LOC107986777
0.882 0.120 7 24200546 intron variant G/A snv 1.4E-03 3
rs9384713
AK9
0.882 0.080 6 109558038 intron variant G/T snv 0.57 3
rs10009128 0.925 0.040 4 19511508 intron variant C/T snv 0.34 2
rs10017335
LOC645513
0.925 0.040 4 119460368 intron variant C/G snv 0.28 2
rs10017573
STX18
0.925 0.040 4 4461337 intron variant T/C snv 0.15 2
rs10019193
LOC107986198 ; DDX60L ; PALLD
0.925 0.040 4 168526369 intron variant G/A;C snv 2
rs10059423
CTNND2
0.925 0.040 5 11600827 intron variant A/C;T snv 2
rs10073216 0.925 0.040 5 169390084 intergenic variant A/G snv 5.1E-02 2
rs10086956
PSKH2 ; ATP6V0D2
0.925 0.040 8 86052433 intron variant C/G snv 0.31 2
rs10103696 0.925 0.040 8 90574875 intron variant G/A snv 0.12 2
rs10112240 0.925 0.040 8 31245931 intergenic variant C/T snv 0.19 2
rs10117057 0.925 0.040 9 7577893 intergenic variant G/A snv 2.8E-02 2
rs10119834 0.925 0.040 9 119037865 intergenic variant C/T snv 0.96 2