Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs55872725
FTO
16 53775211 intron variant C/T snv 0.31 6
rs62434129
PLEKHG1
6 150687701 intron variant A/G;T snv 8.8E-02 6
rs7209400
LOC102724596
1.000 0.040 17 49372695 intron variant C/T snv 0.47 6
rs10184428 2 164155317 intron variant C/A;G snv 5
rs11066015
ACAD10
0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03 5
rs114165349
LOC101928728 ; ARID1A
1 26695422 intron variant G/C snv 1.7E-02 5
rs11636952
LMAN1L
15 74821981 intron variant T/C snv 0.48 5
rs11725969
GUCY1A1
4 155705436 intron variant C/T snv 0.24 5
rs12978472
INSR
19 7257979 intron variant C/G;T snv 5
rs13209747 6 126794309 intron variant C/G;T snv 0.36 5
rs1573643
FURIN
15 90877743 intron variant T/C snv 0.33 5
rs1813353
CACNB2
10 18418519 intron variant T/C snv 0.29 5
rs1894400
FES
15 90885725 intron variant C/T snv 0.28 5
rs2004776
AGT
1 230712956 intron variant C/G;T snv 5
rs2013002 12 111762346 intron variant T/A;C snv 5
rs2043082
ALDH1A2
15 58382109 intron variant G/A snv 0.32 5
rs2304128
GMIP
19 19635342 intron variant G/C;T snv 5
rs2763981
CYP21A2 ; SLC44A4
6 31872244 intron variant T/A snv 0.79 5
rs4495740
DOCK7
1 62658794 intron variant T/G snv 0.34 5
rs6108787 20 10986566 intron variant T/G snv 0.46 5
rs62033406
FTO
16 53790314 intron variant A/G snv 0.33 5
rs6943555
AUTS2
0.882 0.080 7 70341037 intron variant T/A snv 0.34 5