Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 9
rs4760
PLAUR
1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11 8
rs3813565
LOC105370913 ; CHRNB4
0.851 0.080 15 78727268 splice region variant G/A;T snv 6
rs4513061
AGBL1
0.807 0.080 15 86428401 intron variant G/A;T snv 6
rs3124599
NOTCH1
0.851 0.080 9 136509318 intron variant G/A snv 0.13 5
rs36600
MTMR3
0.827 0.080 22 29941597 intron variant T/C snv 0.78 5
rs3787728
LOC100133286 ; CBR1 ; SETD4
0.851 0.080 21 36071595 intron variant T/C snv 0.74 5
rs55853698
CHRNA5
0.882 0.080 15 78565597 5 prime UTR variant T/G snv 0.25 5
rs6790167
TP63
0.827 0.080 3 189869485 intron variant A/G snv 0.53 5
rs397517097
EGFR
0.851 0.080 7 55174777 missense variant T/C snv 4
rs439680 1.000 0.080 5 109998341 regulatory region variant C/G snv 3
rs55985569
MET
0.925 0.080 7 116699588 missense variant G/A;T snv 3.7E-03 3
rs121913297
RB1
1.000 0.080 13 48465028 stop gained G/A;T snv 2
rs1360583020
PXN
1.000 0.080 12 120215202 missense variant G/C snv 4.3E-06 2
rs942190
TDP1 ; EFCAB11
1.000 0.080 14 89956320 intron variant T/C snv 0.37 2
rs10118776
LOC107987046 ; IL33
1.000 0.080 9 6227418 intron variant G/A snv 0.94 1
rs114033761 1.000 0.080 6 31093784 regulatory region variant T/C snv 1
rs117729306
STK33
1.000 0.080 11 8465623 non coding transcript exon variant T/C snv 7.3E-03 1
rs121913295
RB1
1.000 0.080 13 48463741 missense variant G/T snv 1
rs12200782
BTN3A1
1.000 0.080 6 26402808 intron variant C/G snv 7.9E-02 1
rs12666409
DDC
1.000 0.080 7 50567279 upstream gene variant T/A snv 0.21 1
rs12981718
VSTM1
1.000 0.080 19 54064604 upstream gene variant G/A;T snv 1
rs140013431
BMP6
1.000 0.080 6 7770278 intron variant T/C snv 1.2E-02 1
rs141670911 1.000 0.080 6 26581030 intergenic variant A/T snv 7.3E-02 1
rs141877527 1.000 0.080 10 33497992 intergenic variant A/G snv 7.3E-03 1