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: rs2057262
rs2057262
1 1.000 0.036 20 33099326 intron variant C/A snp 0.56 0.010 1.000 1 2007 2007
dbSNP: rs28937873
rs28937873
6 0.821 0.143 15 71813573 missense variant G/A snp 4.0E-04 7.3E-04 0.010 1.000 1 2009 2009
dbSNP: rs1291139
rs1291139
1 1.000 0.036 20 36887791 intron variant A/C,T snp 0.76 0.010 1.000 1 2007 2007