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: rs138308793
rs138308793
1 2 111493181 intron variant G/A snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs62160676
rs62160676
5 2 111410354 intron variant T/C;G snv 0.700 1.000 1 2016 2016