Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 13
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 12
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 10
rs4263839
TNFSF15
0.807 0.160 9 114804160 intron variant A/G snv 0.75 7
rs7869487 0.882 0.040 9 114818634 intergenic variant C/G;T snv 3
rs4662344
ARHGAP15
0.925 0.080 2 143591289 intron variant T/C snv 0.82 3
rs7609897
COLQ
0.925 0.080 3 15461174 intron variant G/T snv 0.22 3
rs67153654
FAM155A
0.925 0.080 13 107572636 intron variant T/A;C snv 3
rs17636410 1.000 0.040 9 72401105 intergenic variant G/A;C snv 1
rs1945615
CALCB
1.000 0.040 11 15081931 3 prime UTR variant G/A snv 0.23 1
rs9514637
FAM155A
1.000 0.040 13 107249894 intron variant G/A snv 0.19 1
rs761545809
PDE7B
1.000 0.040 6 136194523 3 prime UTR variant GAA/- delins 7.5E-04 1
rs2272901
TAB2
1.000 0.040 6 149218637 non coding transcript exon variant G/A snv 0.22 1