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: rs1193
rs1193
2 2 86775106 3 prime UTR variant C/T snv 0.68 0.700 1.000 1 2016 2016
dbSNP: rs4832312
rs4832312
3 2 86762839 intron variant G/A;C snv 0.700 1.000 1 2016 2016