Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 18
rs1131691029
TP53
0.827 0.160 17 7673794 missense variant C/G snv 2
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 1