Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs754820004
CUL3
2 224557736 missense variant T/C snv 4.0E-06 1
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
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
rs777169839
PPARGC1A
4 23828453 missense variant T/C;G snv 2.4E-05 2
rs587780076
TP53
17 7673743 missense variant C/A;T snv 8.0E-06; 8.0E-06 2
rs1802710
DLK1
14 100734308 synonymous variant T/A;C snv 0.63 3
rs1057519887
EGFR
0.925 0.040 7 55154128 missense variant GC/AA;AT mnv 3
rs1057519888
EGFR
0.925 0.080 7 55143386 missense variant A/G snv 3
rs139236063
EGFR
0.925 0.080 7 55165350 missense variant G/C;T snv 3
rs769696078
EGFR
0.925 0.040 7 55154128 missense variant G/A snv 3
rs397516813
RAF1
0.925 0.160 3 12599717 missense variant C/G 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
rs766727892
TCF7L2
0.925 0.040 10 113151107 missense variant G/A snv 1.2E-05 7.0E-06 3
rs1476157710
WNT10B
0.925 0.040 12 48970460 missense variant T/C snv 4.1E-06 1.4E-05 3
rs113994088
ALK
0.925 0.080 2 29222584 missense variant C/G snv 4
rs113994089
ALK
0.925 0.120 2 29220776 missense variant C/G;T snv 4
rs80359183
BRCA2
0.882 0.120 13 32380096 stop gained T/A;C snv 4
rs757066045
CDKN2A
0.882 0.040 9 21974725 missense variant C/T snv 8.2E-06 4
rs1200941109
MYCN ; MYCNOS
0.882 0.040 2 15940679 frameshift variant C/-;CC delins 4
rs1367644026
KRT5
0.925 0.080 12 52520259 missense variant C/A;T snv 4.0E-06 5
rs374052197
PDPN
0.882 0.040 1 13610421 missense variant G/A;T snv 8.0E-06 5