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: rs57961569
rs57961569
5 0.827 0.200 2 15939643 intron variant G/A;C snv 0.010 1.000 1 2018 2018
dbSNP: rs60226897
rs60226897
3 0.882 0.080 2 15947252 downstream gene variant G/A snv 4.3E-02 0.010 1.000 1 2018 2018
dbSNP: rs9653226
rs9653226
3 0.882 0.080 2 15939632 intron variant C/T snv 0.54 0.010 1.000 1 2018 2018