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: rs4100654
rs4100654
3 9 104906960 intron variant T/C snv 8.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs4149269
rs4149269
3 9 104884840 intron variant A/G snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs4149272
rs4149272
3 9 104880006 intron variant C/G;T snv 0.48 0.700 1.000 1 2012 2012
dbSNP: rs4149273
rs4149273
3 9 104879930 intron variant T/C snv 0.45 0.700 1.000 1 2012 2012