Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913315
STK11
0.882 0.160 19 1220488 missense variant G/A;T snv 5
rs1057520017
STK11
1.000 0.040 19 1220630 missense variant C/T snv 1