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: rs7868992
rs7868992
1 1.000 0.120 9 114228791 intron variant G/A snv 0.63 0.810 1.000 2 2013 2015
dbSNP: rs4979356
rs4979356
1 1.000 0.120 9 114228704 intron variant C/G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs4979357
rs4979357
1 1.000 0.120 9 114228715 intron variant T/A;C snv 0.010 1.000 1 2015 2015