Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1418810723
FN1
0.851 0.080 2 215409981 missense variant A/T snv 8.0E-06 9
rs925489
PTCSC2
0.882 0.080 9 97784318 intron variant C/T snv 0.71 6
rs1248131654
RBMS1
0.851 0.080 2 160367217 missense variant G/A snv 1.4E-05 4
rs1443434
FOXE1
0.851 0.080 9 97855197 3 prime UTR variant G/T snv 0.63 4
rs2622590
XKR4
0.925 0.080 8 55445714 intron variant G/A snv 0.15 4
rs28937584
TSHR ; LOC101928462
0.925 0.080 14 81143955 missense variant G/A;C snv 4.0E-06 4
rs360717
IL18
0.851 0.080 11 112164002 5 prime UTR variant G/A snv 0.25 4
rs4987206
RAD52
0.851 0.080 12 916703 missense variant G/C snv 2.4E-03 9.6E-03 4
rs768891111
XRCC3 ; KLC1
0.851 0.080 14 103699474 stop gained C/A;G;T snv 4.0E-06; 4.0E-06 4
rs996807218
KIDINS220
0.882 0.080 2 8827045 missense variant T/C snv 4
rs11466653
TLR10
1.000 0.080 4 38774614 missense variant A/G snv 6.4E-02 4.1E-02 3
rs2296675
MGMT
1.000 0.080 10 129766734 intron variant A/G snv 0.13 3
rs375878504
LOC101059906 ; HRAS ; LRRC56
1.000 0.080 11 532741 synonymous variant G/A;C snv 8.1E-06 7.0E-06 3
rs4915076
VAV3
0.882 0.080 1 107816883 intron variant T/C snv 9.1E-02 3
rs537209983
NKX2-1 ; NKX2-1-AS1 ; SFTA3
0.882 0.080 14 36517378 missense variant G/A snv 1.7E-04 8.4E-05 3
rs11175834
LINC02454 ; LOC100507065
0.925 0.080 12 65598856 intron variant C/T snv 0.14 2
rs11246050
NLRP6
1.000 0.080 11 284257 synonymous variant G/A;C snv 0.16; 4.0E-06 2
rs11575688
HABP2
0.925 0.080 10 113583298 missense variant G/C snv 1.0E-02 1.1E-02 2
rs11762469
BRAF
1.000 0.080 7 140914412 intron variant A/G;T snv 2
rs12990503
DIRC3
0.925 0.080 2 217429494 intron variant C/G snv 0.64 2
rs1347591
NUP93
1.000 0.080 16 56834788 intron variant A/G snv 0.47 0.47 2
rs140451238
ITK
1.000 0.080 5 157208978 synonymous variant T/C snv 1.6E-04 7.8E-04 2
rs1410727652
SLC22A3
1.000 0.080 6 160348669 missense variant C/T snv 7.0E-06 2
rs1453167097
TP53
0.925 0.080 17 7675172 missense variant A/C snv 2
rs1800812
PDGFRA
1.000 0.080 4 54228462 intron variant G/C;T snv 2