Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs373191257
AMFR
0.827 0.080 16 56363027 missense variant T/A snv 1.6E-05 7.0E-06 5
rs766265850
MIR4640 ; DDR1
0.851 0.040 6 30889239 missense variant G/A snv 8.1E-06 7.0E-06 4
rs373584770
CASP1
0.827 0.120 11 105030337 missense variant G/A snv 4.0E-06 7.0E-06 5
rs1306185959
FGFR1
0.851 0.040 8 38429805 missense variant T/C snv 7.0E-06 4
rs371409680
TP53
0.790 0.120 17 7673772 missense variant C/G;T snv 4.0E-05 7.0E-06 10
rs200187877
PPARGC1A
0.851 0.040 4 23795829 missense variant C/T snv 8.0E-06 7.0E-06 4
rs1205454520
KLLN ; PTEN
0.763 0.120 10 87864059 5 prime UTR variant -/G delins 7.2E-06 10
rs769809364
TP73
0.807 0.080 1 3732940 missense variant G/A snv 8.5E-06 1.4E-05 7
rs375391381
FRMD5
0.851 0.040 15 43883735 missense variant C/T snv 8.0E-06 1.4E-05 4
rs771563543
ZEB1
0.851 0.040 10 31510841 missense variant G/A snv 4.0E-06 1.4E-05 5
rs745542298
TP73
0.807 0.080 1 3732781 missense variant G/A;T snv 8.6E-06; 4.3E-06 2.1E-05 6
rs572480837
POU5F1 ; TCF19
0.851 0.040 6 31165582 missense variant T/A snv 5.0E-04 8.4E-05 4
rs55819519
TP53
0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 40
rs118101777
IDH2
0.614 0.280 15 90087472 missense variant C/T snv 2.0E-03 1.6E-03 42
rs2234248
LOC105375056 ; TREM2
0.827 0.040 6 41163980 upstream gene variant A/G snv 2.2E-03 5
rs2904551
PRODH
0.776 0.160 22 18918421 missense variant A/G snv 5.2E-03 2.8E-03 8
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs3024994
VEGFA
0.776 0.120 6 43775770 non coding transcript exon variant C/T snv 3.8E-02 8
rs16906252
MGMT
0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 19
rs11554137
IDH1
0.742 0.040 2 208248468 synonymous variant G/A snv 5.1E-02 6.8E-02 13
rs17296479 0.851 0.040 5 81411157 non coding transcript exon variant T/A snv 9.4E-02 5
rs3092993
ATM ; C11orf65
0.827 0.040 11 108364388 intron variant C/A snv 0.11 5
rs3856806
PPARG
0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs1801320
RAD51 ; RAD51-AS1
0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12 15
rs144551722 0.851 0.040 X 43632629 intergenic variant G/A snv 0.13 4