Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4711998
IL17A
0.708 0.360 6 52185555 upstream gene variant A/G snv 0.64 16
rs2072472
IL1R2
0.732 0.200 2 102026557 intron variant A/G snv 0.24 13
rs465498
CLPTM1L
0.776 0.200 5 1325688 non coding transcript exon variant A/G snv 0.46 9
rs753955
LOC105370113
0.776 0.120 13 23719720 regulatory region variant A/G snv 0.50 9
rs10509670
PLCE1
0.851 0.080 10 94308190 intron variant A/G snv 0.30 5
rs13016963
FLACC1
0.851 0.080 2 201298088 intron variant A/G snv 0.59 5
rs3781264
PLCE1
0.851 0.120 10 94310618 intron variant A/G snv 0.25 5
rs2320615
NAF1
0.925 0.080 4 163148797 intron variant A/G snv 0.78 3
rs2847281
PTPN2
1.000 0.040 18 12821594 intron variant A/G snv 0.32 3
rs750408412
CYP2E1
0.925 0.080 10 133538938 missense variant A/G snv 3
rs776933870
PLCE1
0.925 0.080 10 94306632 missense variant A/G snv 8.0E-06 3
rs917870680
MDM2
0.925 0.080 12 68839304 missense variant A/G snv 3
rs3805322
ADH4 ; LOC100507053
1.000 0.080 4 99135847 intron variant A/G snv 1.1E-02 2
rs7578456 1.000 0.080 2 201370625 intergenic variant A/G snv 0.57 2
rs10191793
ST6GAL2
2 106809420 intron variant A/G snv 0.21 1
rs10201587
FLACC1
2 201338068 intron variant A/G snv 0.47 1
rs11065783
LOC105369980 ; LINC01405
12 110958445 non coding transcript exon variant A/G snv 1.9E-02 1
rs11843987
TFDP1
13 113589954 intron variant A/G snv 9.1E-02 1
rs11972901 7 85966605 intergenic variant A/G snv 0.47 1
rs1346291
LOC105375925
8 81339729 regulatory region variant A/G snv 0.78 1
rs1737076 6 29757544 intron variant A/G snv 0.45 1
rs17450420 13 104386796 intergenic variant A/G snv 5.9E-02 1
rs2110690
FLACC1
2 201320409 intron variant A/G snv 0.42 1
rs7579792
FLACC1
2 201335727 intron variant A/G snv 0.86 1
rs7582362
FLACC1
2 201311571 intron variant A/G snv 0.72 1