Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3917225
IL1R1
0.807 0.160 2 102152842 intron variant A/G snv 0.36 6
rs7850258
PTCSC2
0.827 0.200 9 97786731 intron variant A/G snv 0.72 6
rs10759944
PTCSC2
0.925 0.080 9 97794690 intron variant A/G snv 0.72 4
rs145475805
TG
0.882 0.080 8 132887509 missense variant A/G snv 8.8E-05 3.3E-04 4
rs7028661
PTCSC2
0.882 0.080 9 97776188 intron variant A/G snv 0.72 4
rs1032006770
EGFR
0.882 0.080 7 55160171 missense variant A/G snv 4.0E-06 7.0E-06 3
rs180414
SLC38A4
0.882 0.080 12 46775115 synonymous variant A/G snv 3.1E-03 3
rs7037324
LOC112268051
0.882 0.080 9 97896036 regulatory region variant A/G snv 0.71 3
rs7024345
PTCSC2
0.925 0.080 9 97832956 intron variant A/G snv 0.82 2
rs7848973
PTCSC2
0.925 0.080 9 97826557 intron variant A/G snv 0.67 2
rs12129938
PCNX2
1.000 0.080 1 233276815 intron variant A/G snv 0.20 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1136201
ERBB2
0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 23
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 15
rs397517132
EGFR
0.623 0.280 7 55191846 missense variant A/T snv 48
rs1418810723
FN1
0.851 0.080 2 215409981 missense variant A/T snv 8.0E-06 9
rs73227498
EPB41L4A
1.000 0.080 5 112150207 intron variant A/T snv 0.11 1
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs2145418 0.882 0.080 1 118422631 intergenic variant C/A snv 0.78 3
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs3219489
MUTYH
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27 24
rs11693806
DIRC3
0.925 0.120 2 217427435 non coding transcript exon variant C/A;G snv 0.65 2