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: rs311059
rs311059
1 1.000 0.040 Y 2709663 intron variant T/C snv 0.010 1.000 1 2016 2016
dbSNP: rs312257
rs312257
1 1.000 0.040 Y 2740657 intron variant G/A snv 0.010 1.000 1 2016 2016