Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs10052657
PDE4D
0.807 0.120 5 59111944 intron variant C/A snv 0.17 4
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
rs10120294
NDUFA8
0.925 0.040 9 122134810 regulatory region variant A/G snv 0.71 2
rs10122943
GABBR2
0.925 0.040 9 98400981 intron variant C/T snv 6.3E-02 2
rs10136383 0.925 0.040 14 22332649 intron variant C/T snv 6.4E-02 2
rs10141031
NUMB
0.925 0.040 14 73306901 intron variant C/G snv 0.22 2
rs10170968
LOC107985969
0.925 0.040 2 193089825 intergenic variant G/A snv 4.6E-02 2
rs10175478
LINC01122
0.925 0.040 2 58913731 intron variant C/A;T snv 2
rs10177451
LINC00298
0.925 0.040 2 7959627 intron variant G/A snv 4.5E-02 2
rs1018597
FAM155A
0.925 0.040 13 107500213 intron variant T/C snv 5.3E-02 2
rs1019348
LINC02405
0.925 0.040 12 126918181 intron variant T/C snv 5.9E-02 2
rs10195136
DPP10
0.925 0.040 2 115797465 intron variant T/C snv 6.2E-02 2
rs10238767
GALNT11
0.925 0.040 7 152092941 intron variant G/A snv 5.9E-02 2
rs1024036
KIF9
0.925 0.040 3 47276175 intron variant T/A;C;G snv 2
rs10242233 0.925 0.040 7 118986159 intergenic variant T/C;G snv 2