Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1802710
DLK1
14 100734308 synonymous variant T/A;C snv 0.63 3
rs587780076
TP53
17 7673743 missense variant C/A;T snv 8.0E-06; 8.0E-06 2
rs777169839
PPARGC1A
4 23828453 missense variant T/C;G snv 2.4E-05 2
rs1057519828
EGFR
7 55143387 missense variant G/A snv 1
rs1057519829
EGFR
7 55154050 missense variant A/C;G snv 4.0E-06 1
rs63749833
MLH1
3 36996639 missense variant G/T snv 1
rs754820004
CUL3
2 224557736 missense variant T/C snv 4.0E-06 1
rs762584624
MYL2
12 110919162 missense variant C/A snv 4.0E-06 1
rs774265827
VEGFA
6 43780773 missense variant G/A;T snv 8.0E-06; 2.0E-05 1
rs11554137
IDH1
0.742 0.040 2 208248468 synonymous variant G/A snv 5.1E-02 6.8E-02 13
rs374052197
PDPN
0.882 0.040 1 13610421 missense variant G/A;T snv 8.0E-06 5
rs745934102
PDPN
0.882 0.040 1 13607281 missense variant G/A snv 3.2E-05 1.4E-05 5
rs771563543
ZEB1
0.851 0.040 10 31510841 missense variant G/A snv 4.0E-06 1.4E-05 5
rs1200941109
MYCN ; MYCNOS
0.882 0.040 2 15940679 frameshift variant C/-;CC delins 4
rs757066045
CDKN2A
0.882 0.040 9 21974725 missense variant C/T snv 8.2E-06 4
rs1057519887
EGFR
0.925 0.040 7 55154128 missense variant GC/AA;AT mnv 3
rs1476157710
WNT10B
0.925 0.040 12 48970460 missense variant T/C snv 4.1E-06 1.4E-05 3
rs766727892
TCF7L2
0.925 0.040 10 113151107 missense variant G/A snv 1.2E-05 7.0E-06 3
rs769696078
EGFR
0.925 0.040 7 55154128 missense variant G/A snv 3
rs867657798
TCF4
0.925 0.040 18 55631366 missense variant G/A;C snv 1.4E-05 3
rs868162712
TCF4
0.925 0.040 18 55279598 missense variant G/A snv 3
rs1057519903
H3-3A
0.683 0.080 1 226064434 missense variant A/T snv 28
rs1057519904
H3C11
0.742 0.080 6 27872233 missense variant T/A snv 17
rs149840192
EGFR
0.807 0.080 7 55154129 missense variant C/A;T snv 7
rs773442580
EGF
0.851 0.080 4 109913367 missense variant T/C;G snv 4.0E-06 7