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: rs732526
rs732526
1 3 58051235 intron variant C/T snv 0.45 0.700 1.000 1 2016 2016
dbSNP: rs732527
rs732527
1 3 58051208 intron variant T/C snv 0.45 0.700 1.000 1 2016 2016