Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6856396
SLC2A9
0.925 0.120 4 10029539 intron variant A/C;T snv 3
rs12506455
SLC2A9
0.925 0.120 4 10029945 intron variant T/A snv 0.43 3
rs10939663
SLC2A9
0.925 0.120 4 10030892 intron variant T/G snv 0.20 3
rs12506122
SLC2A9
0.925 0.120 4 10031914 intron variant C/A snv 0.52 3
rs13146686
SLC2A9
0.925 0.120 4 10033309 intron variant T/C snv 0.52 3
rs11722930
SLC2A9
0.925 0.120 4 10033830 intron variant G/A;C snv 3
rs10006397
SLC2A9
0.925 0.120 4 10034516 non coding transcript exon variant C/A snv 0.78 3
rs76099163
SLC2A9
4 10034522 non coding transcript exon variant T/C snv 2.3E-03 1
rs11727199
SLC2A9
0.925 0.120 4 10034566 non coding transcript exon variant C/T snv 0.42 3
rs3733585
SLC2A9
0.925 0.120 4 10034715 non coding transcript exon variant A/G snv 0.43 3
rs11731110
SLC2A9
0.925 0.120 4 10035722 non coding transcript exon variant T/C snv 0.43 3
rs10939665
SLC2A9
0.925 0.120 4 10036004 non coding transcript exon variant T/C snv 0.43 3
rs10012779
SLC2A9
0.925 0.120 4 10036488 intron variant C/T snv 0.15 3
rs13139055
SLC2A9
0.925 0.120 4 10037300 intron variant G/A;T snv 3
rs13115776
SLC2A9
0.925 0.120 4 10038565 intron variant C/A;G;T snv 3
rs12508991
SLC2A9
0.925 0.120 4 10039480 intron variant C/T snv 0.42 3
rs10029311
SLC2A9
0.925 0.120 4 10039510 intron variant T/C snv 0.14 3
rs7679916
SLC2A9
0.925 0.120 4 10040536 intron variant C/T snv 0.42 3
rs7349721
SLC2A9
0.925 0.120 4 10040938 intron variant A/G;T snv 3
rs13101785
SLC2A9
0.925 0.120 4 10041291 intron variant T/A snv 0.42 3
rs13137343
SLC2A9
0.925 0.120 4 10041404 intron variant C/A snv 0.42 3
rs13110307
SLC2A9
0.925 0.120 4 10042740 intron variant T/A;C snv 3
rs13129453
SLC2A9
0.925 0.120 4 10043160 intron variant T/C snv 0.53 3
rs4529049
SLC2A9
0.925 0.120 4 10043765 intron variant C/T snv 0.52 3
rs4637402
SLC2A9
0.925 0.120 4 10043806 intron variant C/A;T snv 3