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 1.000 0.036 7 155461298 intron variant G/A snp 0.72 0.050 1.000 5 2004 2012
dbSNP: rs1861973
rs1861973
EN2
2 1.000 0.036 7 155461450 intron variant T/C snp 0.72 0.030 1.000 3 2006 2012
dbSNP: rs3735653
rs3735653
EN2
2 1.000 0.036 7 155458738 missense variant C/G,T snp 0.54 0.41 0.020 1.000 2 2004 2010
dbSNP: rs2361689
rs2361689
EN2
1 1.000 0.036 7 155462637 synonymous variant T/C snp 0.36 0.35 0.010 1.000 1 2004 2004