Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918664
TERT
0.851 0.120 5 1254395 missense variant C/T snv 5.2E-05 9.1E-05 4
rs12252
IFITM3
0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs1227756
COL13A1
0.925 0.080 10 69828748 intron variant G/A;C snv 2
rs12304647
MIR196A2 ; HOXC6
0.807 0.160 12 53991163 intron variant A/C snv 0.26 6
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv 23
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs13347
CD44
0.763 0.320 11 35231725 3 prime UTR variant C/A;T snv 12
rs13419896
EPAS1
0.776 0.240 2 46329206 intron variant G/A snv 0.10 8
rs1346044973
TERT
0.851 0.160 5 1294158 missense variant G/A snv 1.1E-05 4
rs1358379
LINC00472 ; MIR30A
0.882 0.160 6 71403739 intron variant T/C snv 6.2E-02 3
rs137853590
PHKG2
0.882 0.160 16 30751140 stop gained C/T snv 4.0E-06 3
rs1396171148
FARSB
0.851 0.200 2 222613892 missense variant T/G snv 5
rs1419129874
FARSB
0.851 0.200 2 222642894 missense variant A/G snv 7.0E-06 5
rs1431315635
HFE ; LOC108783645
0.882 0.120 6 26092928 missense variant C/T snv 4.0E-06 3
rs143175221
LOC108783645 ; HFE
0.827 0.200 6 26092952 missense variant T/C snv 8.4E-04 5.6E-04 5
rs1466642025
FARSB
0.851 0.200 2 222631635 missense variant A/G snv 7.0E-06 5
rs1469557
LOC101929248
0.925 0.120 8 10849291 downstream gene variant C/T snv 0.18 2
rs1485766
VEGFC ; LOC105377555
0.882 0.120 4 176689730 intron variant T/A;G snv 3
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1545224
FABP1
0.925 0.120 2 88124297 3 prime UTR variant A/G snv 0.18 2
rs1553553086
FARSB
0.827 0.280 2 222623699 missense variant C/T snv 9
rs1553554543
FARSB
0.851 0.200 2 222631606 missense variant T/C snv 5
rs1682111
ACYP2
0.742 0.240 2 54200842 intron variant A/T snv 0.56 13