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: rs12728900
rs12728900
LIN28A
1 1.000 0.080 1 26420316 intron variant G/A snv 0.29 0.010 1.000 1 2014 2014