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: rs13096142
rs13096142
1 1.000 0.080 3 46240253 intron variant C/T snv 0.25 0.800 1.000 1 2014 2014
dbSNP: rs13098911
rs13098911
5 0.882 0.200 3 46193709 intron variant C/G;T snv 0.800 1.000 1 2010 2010
dbSNP: rs7616215
rs7616215
2 0.925 0.280 3 46164194 intron variant C/T snv 0.62 0.800 1.000 1 2011 2011
dbSNP: rs67676925
rs67676925
2 0.925 0.200 3 46232768 intron variant T/C snv 5.5E-02 0.700 1.000 1 2016 2016