Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912665
TP53
1.000 0.120 17 7674965 missense variant G/A snv 2.4E-05 7.0E-06 7
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 6
rs1238684646
DICER1
14 95090640 missense variant C/G snv 4.0E-06 2
rs267606985
PTHLH
1.000 12 27963693 missense variant A/G snv 2
rs61764370
KRAS
0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs1801260
CLOCK ; TMEM165
0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 213