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: rs4142110
rs4142110
3 0.925 0.120 13 42180386 intron variant T/C snv 0.34 0.030 1.000 3 2012 2017
dbSNP: rs1170155
rs1170155
2 0.925 0.120 13 42128575 intron variant C/T snv 0.65 0.010 1.000 1 2013 2013
dbSNP: rs17646069
rs17646069
2 0.925 0.120 13 42229127 missense variant T/C snv 4.5E-02 2.7E-02 0.010 1.000 1 2017 2017
dbSNP: rs7981733
rs7981733
2 0.925 0.120 13 42115924 intron variant C/A;T snv 0.010 1.000 1 2013 2013