Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs188917216 4 87951768 regulatory region variant A/C snv 5.5E-03 1
rs346750
MARK4 ; EXOC3L2
19 45233960 intron variant A/C snv 0.41 1
rs4608811
SLC2A9
4 10048051 intron variant A/C snv 0.77 1
rs56106601 9 128008205 intergenic variant A/C snv 9.4E-02 1
rs56230350
NFATC3
16 68133068 intron variant A/C snv 0.13 1
rs57440165
GUSBP2
6 26875738 intron variant A/C snv 5.6E-02 1
rs6829727
SLC2A9
4 10050048 intron variant A/C snv 0.51 1
rs71456318
SLC22A11
11 64565390 non coding transcript exon variant A/C snv 0.39 0.37 1
rs74440730
CUBN
10 16878893 intron variant A/C snv 8.7E-02 1
rs9416703
BICC1
10 58523248 intron variant A/C snv 0.46 1
rs199739 0.925 0.120 6 25960281 upstream gene variant A/C;G snv 0.78 5
rs10031453 0.925 0.120 4 10141035 downstream gene variant A/C;G snv 3
rs10805364 0.925 0.120 4 10273894 intergenic variant A/C;G snv 3
rs11949767
MXD3
1.000 0.080 5 177313243 upstream gene variant A/C;G snv 3
rs13128435 0.925 0.120 4 9722048 intergenic variant A/C;G snv 3
rs2024282 0.925 0.120 4 10248064 intergenic variant A/C;G snv 3
rs4697750 0.925 0.120 4 10350082 intergenic variant A/C;G snv 3
rs4697957 0.925 0.120 4 10180630 regulatory region variant A/C;G snv 3
rs6855489 0.925 0.120 4 10207264 intergenic variant A/C;G snv 3
rs7661209 0.925 0.120 4 10357983 intergenic variant A/C;G snv 3
rs7669444
SLC2A9
0.925 0.120 4 9891953 intron variant A/C;G snv 3
rs7670751
SLC2A9
0.925 0.120 4 9937149 intron variant A/C;G snv 3
rs11730631 4 10291344 downstream gene variant A/C;G snv 1
rs1574430
SLC22A7 ; CRIP3
6 43301291 intron variant A/C;G snv 0.55 1
rs56223908
SLC2A9
4 9916868 intron variant A/C;G snv 5.8E-02 1