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: rs236114
rs236114
MCM8
2 1.000 0.040 20 5954739 intron variant T/C snv 0.84 0.84 0.800 1.000 2 2009 2013