Source: ALL
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 22
rs10213865
LOC105374724 ; IL7R
0.827 0.120 5 35857748 intron variant A/C;T snv 5
rs1023835002
B2M ; PATL2
0.763 0.280 15 44711547 start lost A/G;T snv 10
rs10248565
HDAC9
1.000 0.040 7 18935100 intron variant T/G snv 0.14 3
rs1026411
LOC105375751 ; PCAT1
0.827 0.080 8 127014165 intron variant G/A;C snv 0.25 5
rs1032737355
EGFR
0.925 0.080 7 55170434 missense variant T/A snv 2
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs10429489 0.925 0.080 9 21787522 intergenic variant G/A snv 0.26 2
rs1048155
BHLHE41 ; SSPN
1.000 0.040 12 26120155 3 prime UTR variant C/G snv 0.48 1
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs104886026
EGFR
0.851 0.080 7 55200333 missense variant G/A snv 4
rs104894226
LRRC56 ; HRAS
0.658 0.560 11 534285 missense variant C/A;G;T snv 29
rs104894228
LRRC56 ; HRAS
0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs104894231
LRRC56 ; HRAS
0.776 0.360 11 533467 missense variant C/G;T snv 9
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs104894340
CDK4
0.827 0.200 12 57751647 missense variant C/A;T snv 5
rs1050171
EGFR ; EGFR-AS1
0.851 0.120 7 55181370 missense variant G/A;C snv 0.52; 4.0E-06 6
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs1051753269
EGFR
0.790 0.120 7 55174029 missense variant G/A snv 7.0E-06 7
rs10519198
IREB2
0.925 0.080 15 78450412 intron variant C/A;G snv 2
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1056562
MPZL2
1.000 0.040 11 118254910 3 prime UTR variant T/C snv 0.57 1