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: rs1861972
rs1861972
EN2
2 0.925 0.040 7 155461298 intron variant G/A snv 0.72 0.070 1.000 7 2004 2010
dbSNP: rs1861973
rs1861973
EN2
2 0.925 0.040 7 155461450 intron variant T/C snv 0.73 0.060 1.000 6 2004 2010
dbSNP: rs3735653
rs3735653
EN2
2 0.925 0.040 7 155458738 missense variant C/G;T snv 0.54 0.010 1.000 1 2010 2010
dbSNP: rs3824068
rs3824068
EN2
1 1.000 0.040 7 155460803 intron variant C/T snv 0.34 0.010 1.000 1 2008 2008