Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs116909374 0.776 0.120 14 36269155 regulatory region variant C/T snv 2.3E-02 11
rs11693806
DIRC3
0.925 0.120 2 217427435 non coding transcript exon variant C/A;G snv 0.65 2
rs1169803481
EGFR
0.807 0.160 7 55198851 missense variant A/G snv 4.0E-06 7
rs1179469165
LOC101928462 ; TSHR
0.925 0.080 14 81143917 missense variant C/T snv 8.0E-06 7.0E-06 2
rs12129938
PCNX2
1.000 0.080 1 233276815 intron variant A/G snv 0.20 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121912664
TP53
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 44
rs121913308
RET
0.827 0.120 10 43114492 missense variant A/C;G;T snv 6
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs12348691
PTCSC2
0.925 0.120 9 97846400 intron variant G/A snv 0.63 2
rs1248131654
RBMS1
0.851 0.080 2 160367217 missense variant G/A snv 1.4E-05 4
rs12508721
IL21-AS1
0.742 0.360 4 122623509 intron variant C/T snv 0.24 11
rs12628
LRRC56 ; HRAS
0.776 0.160 11 534242 synonymous variant A/G snv 0.32 0.34 10
rs12769288
MGMT
0.882 0.080 10 129488086 intron variant C/T snv 0.10 3
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs1297812518
LOC112268131 ; KLC1 ; XRCC3
0.763 0.160 14 103707168 missense variant G/A snv 1.3E-05 1.4E-05 9
rs13143866
IL21 ; IL21-AS1
0.851 0.200 4 122619603 intron variant G/A snv 0.24 4
rs1365943053
PTCH1
0.882 0.080 9 95516630 missense variant C/T snv 7.0E-06 3
rs1418810723
FN1
0.851 0.080 2 215409981 missense variant A/T snv 8.0E-06 9
rs142698837
TG
0.851 0.080 8 132869781 missense variant G/A snv 7.6E-04 7.0E-04 5
rs1443434
FOXE1
0.851 0.080 9 97855197 3 prime UTR variant G/T snv 0.63 4
rs1443435
FOXE1
1.000 0.080 9 97855301 3 prime UTR variant T/C snv 0.63 1
rs1443438
PTCSC2
0.827 0.080 9 97787746 intron variant T/A;C snv 8
rs145475805
TG
0.882 0.080 8 132887509 missense variant A/G snv 8.8E-05 3.3E-04 4
rs1503185
PTPRJ
0.807 0.120 11 48125070 missense variant G/A snv 0.18 0.19 8