Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2592555
PRR5L
1.000 0.120 11 36350207 intron variant T/C;G snv 1
rs2897443
RAD50
1.000 0.120 5 132593902 intron variant G/T snv 0.18 1
rs2918307 1.000 0.120 19 8679458 downstream gene variant A/G;T snv 0.19 1
rs370555009
LTC4S
1.000 0.120 5 179794090 missense variant G/A;C snv 1.6E-05; 4.0E-06 1
rs41268896
TNXB
1.000 0.120 6 32102292 intron variant G/A snv 0.25 1
rs4643526
PUS10
1.000 0.120 2 60957516 intron variant G/A snv 0.35 1
rs4674343
CYP27A1
1.000 0.120 2 218795623 intron variant A/G snv 0.48 1
rs471144 1.000 0.120 1 152481779 intergenic variant T/G snv 8.0E-02 1
rs4713555
HLA-DRB1
1.000 0.120 6 32607747 intergenic variant G/T snv 0.28 1
rs4809219
RTEL1 ; RTEL1-TNFRSF6B
1.000 0.120 20 63671762 intron variant C/A;G;T snv 1
rs512685
ZC3H12D
1.000 0.120 6 149471889 intron variant G/A snv 0.15 1
rs55879323
LOC112268240 ; PUDPP2 ; FLG-AS1
1.000 0.120 1 152196264 intron variant C/T snv 0.42 1
rs593982 1.000 0.120 11 65745636 upstream gene variant T/A;C snv 1
rs61813875 1.000 0.120 1 152564174 downstream gene variant C/G snv 1.6E-02 1
rs6419573 1.000 0.120 2 102410643 upstream gene variant T/C snv 0.78 1
rs6602364 1.000 0.120 10 5996890 regulatory region variant G/C snv 0.50 1
rs6661961 1.000 0.120 1 152469813 intergenic variant T/A;C snv 1
rs6686734
MFN2
1.000 0.120 1 12008884 intron variant T/C snv 0.71 1
rs6720763
XIRP2 ; XIRP2-AS1
1.000 0.120 2 167135776 intron variant T/C snv 0.27 1
rs7000782 1.000 0.120 8 80395915 intron variant T/A snv 0.54 1
rs7613051
GLB1 ; LOC107986073
1.000 0.120 3 33023847 intron variant G/A snv 0.25 1
rs7701890
TMEM232
1.000 0.120 5 110523120 intron variant A/G snv 0.15 1
rs77199844
LCE1E
1.000 0.120 1 152784619 upstream gene variant AT/- del 0.12 1
rs7815944
LINC00824
1.000 0.120 8 128415272 intron variant A/G snv 0.12 1
rs9050
TCHH
1.000 0.120 1 152106838 3 prime UTR variant C/A snv 4.3E-02 1