Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs10499563
STEAP1B
0.807 0.120 7 22720869 intron variant T/C snv 0.21 7
rs1050450
GPX1
0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs10509670
PLCE1
0.851 0.080 10 94308190 intron variant A/G snv 0.30 5
rs10511729
LOC101929563
0.742 0.240 9 23557229 intron variant T/G snv 0.35 11
rs10512263
TGFBR1
0.851 0.120 9 99123789 intron variant T/C snv 6.5E-02 4
rs1051690
INSR
0.851 0.080 19 7116952 3 prime UTR variant T/C snv 0.83 4
rs1051740
EPHX1
0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1053023
STAT3
0.882 0.120 17 42313598 3 prime UTR variant T/A;C snv 4
rs1057317
TLR4
0.827 0.160 9 117715764 3 prime UTR variant C/A snv 5
rs1057519847
EGFR
0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs1062935
RPTOR ; LOC400627
0.925 0.080 17 80966057 3 prime UTR variant T/C snv 0.40 2
rs1064261
MTOR
0.925 0.080 1 11228701 missense variant G/A;T snv 0.75; 4.0E-06 3
rs10680577
RAB4B-EGLN2 ; EGLN2
0.776 0.160 19 40798690 intron variant -/TACT delins 10
rs10719
DROSHA
0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
rs10739971
MIRLET7A1 ; MIRLET7F1
0.882 0.080 9 94175398 intron variant G/A;C snv 5
rs10746463
CD55
0.851 0.200 1 207337251 missense variant G/A;T snv 4
rs10787498
CASP7
0.925 0.080 10 113729891 3 prime UTR variant T/G snv 0.38 2
rs10811474 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 11
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs10983755 0.790 0.320 9 117702392 upstream gene variant G/A snv 3.2E-02 7