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: rs142155101
rs142155101
2 0.923 0.107 2 214728728 missense variant C/T snp 1.7E-03 1.8E-03 0.710 1.000 2 1998 2006
dbSNP: rs1047972
rs1047972
15 0.707 0.214 20 56386407 missense variant T/C snp 0.85 0.84 0.010 1.000 1 2007 2007
dbSNP: rs2273535
rs2273535
22 0.679 0.250 20 56386485 missense variant A/C,T snp 0.28 0.23 0.010 1.000 1 2007 2007
dbSNP: rs28930073
rs28930073
7 0.784 0.107 3 37007004 missense variant G/C snp 2.1E-04 0.010 1.000 1 2005 2005