Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 52
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs397516436
TP53
0.641 0.440 17 7674894 stop gained G/A;C snv 26
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 21