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: rs1345514
rs1345514
EN2
1 1.000 0.040 7 155456455 intron variant C/T snv 0.29 0.010 1.000 1 2009 2009
dbSNP: rs3808330
rs3808330
EN2
1 1.000 0.040 7 155463312 3 prime UTR variant T/C snv 0.23 0.010 1.000 1 2009 2009