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: rs2024714
rs2024714
1 20 61637438 intron variant C/T snv 0.60 0.800 1.000 1 2010 2010
dbSNP: rs4468878
rs4468878
1 20 61353181 intron variant T/C snv 0.51 0.800 1.000 1 2010 2010