Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805015
IL4R
0.683 0.520 16 27362859 missense variant T/C snv 0.16 0.22 22
rs121913273
PIK3CA
0.605 0.440 3 179218294 missense variant G/A;C snv 22
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 22
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 21
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 20
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 20
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 20
rs1273593548
PIK3CG
0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 19
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 19
rs121913503
IDH2
0.689 0.200 15 90088606 missense variant C/A;T snv 18
rs121913444
EGFR
0.724 0.160 7 55191831 missense variant T/A;C;G snv 17
rs16906252
MGMT
0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 17
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 16
rs55705857
CCDC26
0.732 0.080 8 129633446 intron variant A/G snv 3.9E-02 15
rs7003908
PRKDC
0.716 0.320 8 47858141 intron variant C/A snv 0.66 15
rs562015640
PTEN
0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 15
rs1057519904
H3C11
0.742 0.080 6 27872233 missense variant T/A snv 14
rs1801320
RAD51 ; RAD51-AS1
0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12 14
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 14
rs1057519902
H3-3A
0.742 0.160 1 226064451 missense variant G/C snv 13
rs1553260624
H3-3A
0.763 0.080 1 226064454 missense variant G/A snv 13
rs11554137
IDH1
0.742 0.040 2 208248468 synonymous variant G/A snv 5.1E-02 6.8E-02 13
rs4644
LGALS3
0.732 0.320 14 55138217 missense variant C/A;G snv 0.35 13
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 13