Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs137853077
rs137853077
STK11
2 1.000 0.160 19 1207113 missense variant T/C snv 0.810 1.000 11 1998 2019