Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 18
rs1023835002
B2M ; PATL2
0.763 0.280 15 44711547 start lost A/G;T snv 10
rs10429489 0.925 0.080 9 21787522 intergenic variant G/A snv 0.26 2
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 34
rs104894226
LRRC56 ; HRAS
0.658 0.560 11 534285 missense variant C/A;G;T snv 23
rs104894228
LRRC56 ; HRAS
0.605 0.560 11 534286 missense variant C/A;G;T snv 30
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 52
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 36
rs104894231
LRRC56 ; HRAS
0.776 0.360 11 533467 missense variant C/G;T snv 7
rs104894340
CDK4
0.827 0.200 12 57751647 missense variant C/A;T snv 5
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 11
rs10519198
IREB2
0.925 0.080 15 78450412 intron variant C/A;G snv 2
rs1056562
MPZL2
1.000 0.040 11 118254910 3 prime UTR variant T/C snv 0.57 1
rs1057519045
FGFR2
0.851 0.160 10 121498522 missense variant T/G snv 6
rs1057519720
BRAF
0.851 0.080 7 140781602 missense variant CC/AA;GA mnv 2
rs1057519728
MAP2K1
0.851 0.120 15 66435103 missense variant T/A;C;G snv 5
rs1057519731
MAP2K1
0.925 0.040 15 66436816 missense variant G/C snv 2
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
rs1057519781
ALK
0.807 0.160 2 29209816 missense variant C/G snv 1
rs1057519782
ALK
1.000 0.040 2 29220734 missense variant G/T snv 1
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 1
rs1057519784
ALK
0.827 0.080 2 29220765 missense variant G/T snv 1
rs1057519785
ALK
1.000 0.040 2 29222404 missense variant A/C snv 1
rs1057519786
ARAF
0.882 0.160 X 47566722 missense variant C/G;T snv 3
rs1057519787
ERBB2
1.000 0.040 17 39711952 missense variant G/A;C snv 2