Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913444
EGFR
0.724 0.160 7 55191831 missense variant T/A;C;G snv 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
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
rs121909218
PTEN
0.672 0.360 10 87933145 missense variant G/A snv 12
rs3788266
S100B
0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50 12
rs74315452
SOD1
0.732 0.160 21 31667356 missense variant T/C snv 12
rs11196067
VTI1A
0.752 0.160 10 112709306 intron variant A/T snv 0.32 10
rs1205454520
KLLN ; PTEN
0.763 0.120 10 87864059 5 prime UTR variant -/G delins 7.2E-06 10
rs869320694
FGFR1
0.742 0.520 8 38414790 missense variant T/C snv 10
rs2243248
IL4
0.763 0.240 5 132672952 upstream gene variant T/A;C;G snv 9
rs2293157
STAT5A
0.763 0.120 17 42300657 intron variant C/A;T snv 9
rs2297440
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.080 20 63680946 intron variant T/C snv 0.81 9
rs397516436
TP53
0.641 0.440 17 7674894 stop gained G/A;C snv 9
rs4295627
CCDC26
0.763 0.200 8 129673211 intron variant T/G snv 0.17 9
rs786204929
PTEN
0.752 0.200 10 87933144 stop gained G/A;T snv 9
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 8
rs28929495
EGFR
0.807 0.120 7 55174014 missense variant G/A;C;T snv 8
rs3024994
VEGFA
0.776 0.120 6 43775770 non coding transcript exon variant C/T snv 3.8E-02 8
rs498872
PHLDB1
0.776 0.240 11 118606652 5 prime UTR variant A/G;T snv 8